IL96435A - 6-Aryl-5,6-dihydroimidazo [2,1-b]thiazole derivatives, their preparation and pharmaceutical compositions containing them. - Google Patents

6-Aryl-5,6-dihydroimidazo [2,1-b]thiazole derivatives, their preparation and pharmaceutical compositions containing them.

Info

Publication number: IL96435A
Authority: IL; Israel
Prior art keywords: formula; thiazole; compound; dihydro; compounds
Prior art date: 1989-11-24

Application number

IL9643590A

Other languages

English (en)

Other versions

IL96435A0 (en

Original Assignee

Janssen Pharmaceutica Nv

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1989-11-24

Filing date

1990-11-22

Publication date

1995-03-15

1990-11-22 Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv

1990-11-22 Priority to IL10965190A priority Critical patent/IL109651A/en

1991-08-16 Publication of IL96435A0 publication Critical patent/IL96435A0/xx

1994-05-13 Priority to IL10965194A priority patent/IL109651A0/xx

1995-03-15 Publication of IL96435A publication Critical patent/IL96435A/en

Links

239000008194 pharmaceutical composition Substances 0.000 title abstract description 8
238000002360 preparation method Methods 0.000 title description 11
150000001875 compounds Chemical class 0.000 claims abstract description 79
-1 nitro, amino Chemical group 0.000 claims abstract description 49
239000002253 acid Substances 0.000 claims abstract description 28
150000003839 salts Chemical class 0.000 claims abstract description 20
230000003308 immunostimulating effect Effects 0.000 claims abstract description 15
238000000034 method Methods 0.000 claims abstract description 14
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 10
125000003118 aryl group Chemical group 0.000 claims abstract description 9
239000004480 active ingredient Substances 0.000 claims abstract description 8
125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims abstract description 7
125000002541 furyl group Chemical group 0.000 claims abstract description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 6
239000001257 hydrogen Substances 0.000 claims abstract description 6
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
125000004658 aryl carbonyl amino group Chemical group 0.000 claims abstract description 5
125000004076 pyridyl group Chemical group 0.000 claims abstract description 5
125000001544 thienyl group Chemical group 0.000 claims abstract description 5
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 4
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims abstract description 3
ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 claims abstract description 3
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims abstract description 3
PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 claims abstract description 3
125000001475 halogen functional group Chemical group 0.000 claims abstract 7
239000000203 mixture Substances 0.000 claims description 38
FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 24
239000003153 chemical reaction reagent Substances 0.000 claims description 17
239000012442 inert solvent Substances 0.000 claims description 12
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
239000002585 base Substances 0.000 claims description 9
125000001424 substituent group Chemical group 0.000 claims description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
239000003513 alkali Substances 0.000 claims description 4
WRYCSMQKUKOKBP-UHFFFAOYSA-N Imidazolidine Chemical compound C1CNCN1 WRYCSMQKUKOKBP-UHFFFAOYSA-N 0.000 claims description 3
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 3
125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims description 3
230000003213 activating effect Effects 0.000 claims description 3
239000003814 drug Substances 0.000 claims description 3
239000012458 free base Substances 0.000 claims description 3
230000005526 G1 to G0 transition Effects 0.000 claims description 2
125000004093 cyano group Chemical group *C#N 0.000 claims description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
125000003837 (C1-C20) alkyl group Chemical group 0.000 abstract 1
125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 1
125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
MBVFRSJFKMJRHA-UHFFFAOYSA-N 4-fluoro-1-benzofuran-7-carbaldehyde Chemical group FC1=CC=C(C=O)C2=C1C=CO2 MBVFRSJFKMJRHA-UHFFFAOYSA-N 0.000 abstract 1
125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
239000000543 intermediate Substances 0.000 description 46
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 39
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 37
239000000243 solution Substances 0.000 description 31
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 27
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 24
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 23
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 18
125000000896 monocarboxylic acid group Chemical group 0.000 description 17
239000002904 solvent Substances 0.000 description 16
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
238000003756 stirring Methods 0.000 description 13
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
125000001246 bromo group Chemical group Br* 0.000 description 12
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 12
239000011541 reaction mixture Substances 0.000 description 11
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 10
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
229960001701 chloroform Drugs 0.000 description 10
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 10
150000007513 acids Chemical class 0.000 description 9
239000000047 product Substances 0.000 description 9
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 9
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 8
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
230000000118 anti-neoplastic effect Effects 0.000 description 8
201000010099 disease Diseases 0.000 description 8
125000005843 halogen group Chemical group 0.000 description 8
239000003826 tablet Substances 0.000 description 8
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
150000004945 aromatic hydrocarbons Chemical class 0.000 description 7
238000006243 chemical reaction Methods 0.000 description 7
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 7
238000002560 therapeutic procedure Methods 0.000 description 7
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 6
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
MUBZPKHOEPUJKR-UHFFFAOYSA-L Oxalate Chemical compound [O-]C(=O)C([O-])=O MUBZPKHOEPUJKR-UHFFFAOYSA-L 0.000 description 6
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical class OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
125000004432 carbon atom Chemical group C* 0.000 description 6
125000001309 chloro group Chemical group Cl* 0.000 description 6
HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical compound OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 description 6
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
238000010992 reflux Methods 0.000 description 6
238000012360 testing method Methods 0.000 description 6
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 5
108010062580 Concanavalin A Proteins 0.000 description 5
HLFSDGLLUJUHTE-SNVBAGLBSA-N Levamisole Chemical compound C1([C@H]2CN3CCSC3=N2)=CC=CC=C1 HLFSDGLLUJUHTE-SNVBAGLBSA-N 0.000 description 5
235000011114 ammonium hydroxide Nutrition 0.000 description 5
229950005499 carbon tetrachloride Drugs 0.000 description 5
150000008282 halocarbons Chemical class 0.000 description 5
238000010438 heat treatment Methods 0.000 description 5
229960001614 levamisole Drugs 0.000 description 5
239000000376 reactant Substances 0.000 description 5
238000007363 ring formation reaction Methods 0.000 description 5
239000000725 suspension Substances 0.000 description 5
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 5
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
239000002202 Polyethylene glycol Substances 0.000 description 4
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric Acid Chemical compound [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
239000002246 antineoplastic agent Substances 0.000 description 4
229940041181 antineoplastic drug Drugs 0.000 description 4
239000000010 aprotic solvent Substances 0.000 description 4
239000002775 capsule Substances 0.000 description 4
238000001816 cooling Methods 0.000 description 4
208000035475 disorder Diseases 0.000 description 4
239000003480 eluent Substances 0.000 description 4
150000002170 ethers Chemical class 0.000 description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 4
150000002576 ketones Chemical class 0.000 description 4
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 4
229920001223 polyethylene glycol Polymers 0.000 description 4
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical compound C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
229920002472 Starch Polymers 0.000 description 3
239000000654 additive Substances 0.000 description 3
229910052783 alkali metal Inorganic materials 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
230000037396 body weight Effects 0.000 description 3
238000002512 chemotherapy Methods 0.000 description 3
150000004985 diamines Chemical class 0.000 description 3
229960001760 dimethyl sulfoxide Drugs 0.000 description 3
239000003937 drug carrier Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
229940052308 general anesthetics halogenated hydrocarbons Drugs 0.000 description 3
UVNXNSUKKOLFBM-UHFFFAOYSA-N imidazo[2,1-b][1,3,4]thiadiazole Chemical group N1=CSC2=NC=CN21 UVNXNSUKKOLFBM-UHFFFAOYSA-N 0.000 description 3
238000010348 incorporation Methods 0.000 description 3
239000007788 liquid Substances 0.000 description 3
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 3
239000002609 medium Substances 0.000 description 3
150000007524 organic acids Chemical class 0.000 description 3
235000005985 organic acids Nutrition 0.000 description 3
230000000144 pharmacologic effect Effects 0.000 description 3
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000002244 precipitate Substances 0.000 description 3
239000012279 sodium borohydride Substances 0.000 description 3
229910000033 sodium borohydride Inorganic materials 0.000 description 3
229910000029 sodium carbonate Inorganic materials 0.000 description 3
239000012453 solvate Substances 0.000 description 3
235000019698 starch Nutrition 0.000 description 3
239000007858 starting material Substances 0.000 description 3
RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical compound NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 description 2
HPYNZHMRTTWQTB-UHFFFAOYSA-N 2,3-dimethylpyridine Chemical compound CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 2
238000010600 3H thymidine incorporation assay Methods 0.000 description 2
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 2
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108091003079 Bovine Serum Albumin Proteins 0.000 description 2
COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 description 2
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 2
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 2
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
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SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 2
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KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
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DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
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IQFYYKKMVGJFEH-XLPZGREQSA-N Thymidine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](O)C1 IQFYYKKMVGJFEH-XLPZGREQSA-N 0.000 description 2
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229910000147 aluminium phosphate Inorganic materials 0.000 description 2
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
238000009835 boiling Methods 0.000 description 2
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MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
238000004587 chromatography analysis Methods 0.000 description 2
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238000000576 coating method Methods 0.000 description 2
238000004440 column chromatography Methods 0.000 description 2
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239000012894 fetal calf serum Substances 0.000 description 2
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/40—Unsubstituted amino or imino radicals
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Immunology (AREA)
Medicinal Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Pharmacology & Pharmacy (AREA)
Bioinformatics & Cheminformatics (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Thiazole And Isothizaole Compounds (AREA)

IL9643590A 1989-11-24 1990-11-22 6-Aryl-5,6-dihydroimidazo [2,1-b]thiazole derivatives, their preparation and pharmaceutical compositions containing them. IL96435A (en)

Priority Applications (2)

Application Number	Priority Date	Filing Date	Title
IL10965190A IL109651A (en)	1989-11-24	1990-11-22	2-(3h)- Iminothiazoel derivatives
IL10965194A IL109651A0 (en)	1989-11-24	1994-05-13	2-Iminothiazole derivatives

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US44084289A	1989-11-24	1989-11-24

Publications (2)

Publication Number	Publication Date
IL96435A0 IL96435A0 (en)	1991-08-16
IL96435A true IL96435A (en)	1995-03-15

Family

ID=23750399

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL9643590A IL96435A (en)	1989-11-24	1990-11-22	6-Aryl-5,6-dihydroimidazo [2,1-b]thiazole derivatives, their preparation and pharmaceutical compositions containing them.

Country Status (25)

Country	Link
EP (1)	EP0430334B1 (de)
JP (1)	JPH03170487A (de)
KR (1)	KR910009714A (de)
CN (1)	CN1032754C (de)
AT (1)	ATE127795T1 (de)
AU (1)	AU630766B2 (de)
BG (1)	BG60587B1 (de)
CA (1)	CA2028756A1 (de)
CZ (1)	CZ281422B6 (de)
DE (1)	DE69022370T2 (de)
FI (1)	FI93459C (de)
HU (1)	HU206361B (de)
IE (1)	IE67656B1 (de)
IL (1)	IL96435A (de)
MY (1)	MY131024A (de)
NO (1)	NO300065B1 (de)
NZ (1)	NZ236026A (de)
PL (1)	PL165413B1 (de)
PT (1)	PT95978B (de)
RO (1)	RO108869B1 (de)
RU (1)	RU2051153C1 (de)
YU (1)	YU47955B (de)
ZA (1)	ZA909445B (de)
ZM (1)	ZM5390A1 (de)
ZW (1)	ZW17890A1 (de)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0524055A1 (de) *	1991-07-19	1993-01-20	Synthelabo	Imidazo(2,1-b)benzothiazolderivate, Verfahren zu ihrer Herstellung und ihre therapeutische Verwendung
US6165253A (en) *	1994-05-23	2000-12-26	New Jersey Institute Of Technology	Apparatus for removal of volatile organic compounds from gaseous mixtures
RU2129870C1 (ru) *	1998-04-07	1999-05-10	Ливицкий Василий Иванович	Способ получения антимикробного и противоопухолевого лечебного средства
ATE380548T1 (de)	1999-01-29	2007-12-15	Univ Illinois	Verwendung von p53 inhibitoren zur behandlung von nebenerscheinungen bei der krebstherapie
EP1797880A3 (de) *	1999-01-29	2010-04-28	Board Of Trustees Of The University Of Illinois	Verwendung von P53-Hemmern zur Behandlung der Nebenwirkungen der Krebsbehandlung
BRPI0516177B8 (pt)	2004-09-28	2021-05-25	Quark Biotech Inc	oligorribonucleotídeos, uso dos mesmos, uso de um composto sirna eficaz para inibir 0 p53 humano e composição farmacêutica que os contém, bem como método para diminuição da expressão do gene p53
RU2282438C1 (ru) *	2005-03-24	2006-08-27	Александра Петровна Безрукова	Средство, обладающее противоопухолевой активностью
US7825099B2 (en)	2006-01-20	2010-11-02	Quark Pharmaceuticals, Inc.	Treatment or prevention of oto-pathologies by inhibition of pro-apoptotic genes
US7910566B2 (en)	2006-03-09	2011-03-22	Quark Pharmaceuticals Inc.	Prevention and treatment of acute renal failure and other kidney diseases by inhibition of p53 by siRNA
DK2170403T3 (da)	2007-06-27	2014-06-16	Quark Pharmaceuticals Inc	Sammensætninger og fremgangsmåder til hæmning af ekspressionen af proapoptotiske gener
CN104557979A (zh) *	2013-10-23	2015-04-29	丹阳恒安化学科技研究所有限公司	盐酸左旋咪唑的制备方法
RU2763739C1 (ru) *	2021-06-28	2021-12-30	Федеральное государственное автономное образовательное учреждение высшего образования "Пермский государственный национальный исследовательский университет" (ПГНИУ)	(Z)-9-ароил-8-гидрокси-6-(2-гидроксифенил)-2-(((Z)-2-оксоиндолин-3-илиден)гидразоно)-1-тиа-3,6-диазаспиро[4.4]нон-8-ен-4,7-дионы, обладающие противомикробной активностью
JP7814782B2 (ja) *	2021-11-29	2026-02-17	オーシャンユニバーシティオブチャイナ	イミダゾチアゾール誘導体およびその製造方法と使用

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU409983B2 (en) *	1965-07-19	1970-12-31	Imperial Chemical Industries Of Australia New Zealand Limited	Process for the manufacture of thia zolidines and thiazolidines produced thereby
GB1444743A (en) *	1973-09-20	1976-08-04	Pfizer Ltd	7-substituted imidazo-1,1-b-thiazolium and 9-substituted thiazolo-3,2-a-benzimidazolium derivatives having hypogly caemic and/or growth promotant properties
US4340738A (en) *	1979-06-21	1982-07-20	Janssen Pharmaceutica, N.V.	2,3-Dihydro-imidazo[2,1-b]benzothiazoles

1990
- 1990-10-29 CA CA002028756A patent/CA2028756A1/en not_active Abandoned
- 1990-11-09 NZ NZ236026A patent/NZ236026A/xx unknown
- 1990-11-15 DE DE69022370T patent/DE69022370T2/de not_active Expired - Fee Related
- 1990-11-15 AT AT90203031T patent/ATE127795T1/de active
- 1990-11-15 EP EP90203031A patent/EP0430334B1/de not_active Expired - Lifetime
- 1990-11-17 JP JP2310193A patent/JPH03170487A/ja active Pending
- 1990-11-20 YU YU220890A patent/YU47955B/sh unknown
- 1990-11-21 AU AU66809/90A patent/AU630766B2/en not_active Ceased
- 1990-11-21 MY MYPI90002052A patent/MY131024A/en unknown
- 1990-11-22 BG BG93298A patent/BG60587B1/bg unknown
- 1990-11-22 IL IL9643590A patent/IL96435A/en not_active IP Right Cessation
- 1990-11-22 CZ CS905803A patent/CZ281422B6/cs unknown
- 1990-11-23 RO RO146390A patent/RO108869B1/ro unknown
- 1990-11-23 ZW ZW178/90A patent/ZW17890A1/xx unknown
- 1990-11-23 ZM ZM53/90A patent/ZM5390A1/xx unknown
- 1990-11-23 FI FI905788A patent/FI93459C/fi not_active IP Right Cessation
- 1990-11-23 PT PT95978A patent/PT95978B/pt not_active IP Right Cessation
- 1990-11-23 NO NO905086A patent/NO300065B1/no unknown
- 1990-11-23 RU SU904831684A patent/RU2051153C1/ru active
- 1990-11-23 PL PL90287907A patent/PL165413B1/pl unknown
- 1990-11-23 KR KR1019900019029A patent/KR910009714A/ko not_active Ceased
- 1990-11-23 IE IE424190A patent/IE67656B1/en not_active IP Right Cessation
- 1990-11-23 ZA ZA909445A patent/ZA909445B/xx unknown
- 1990-11-23 HU HU907633A patent/HU206361B/hu not_active IP Right Cessation
- 1990-11-24 CN CN90109407A patent/CN1032754C/zh not_active Expired - Fee Related

Also Published As

Publication number	Publication date
IE904241A1 (en)	1991-06-05
RO108869B1 (ro)	1994-09-30
DE69022370T2 (de)	1996-03-14
PT95978A (pt)	1991-09-13
PL287907A1 (en)	1992-04-21
YU47955B (sh)	1996-07-24
EP0430334B1 (de)	1995-09-13
FI93459B (fi)	1994-12-30
PL165413B1 (pl)	1994-12-30
CZ580390A3 (en)	1996-06-12
NZ236026A (en)	1992-03-26
BG93298A (bg)	1993-12-24
AU6680990A (en)	1991-05-30
ATE127795T1 (de)	1995-09-15
HU907633D0 (en)	1991-06-28
IE67656B1 (en)	1996-04-17
BG60587B1 (bg)	1995-09-29
EP0430334A1 (de)	1991-06-05
RU2051153C1 (ru)	1995-12-27
FI905788A0 (fi)	1990-11-23
KR910009714A (ko)	1991-06-28
MY131024A (en)	2007-07-31
NO905086D0 (no)	1990-11-23
ZW17890A1 (en)	1992-07-08
ZA909445B (en)	1992-07-29
IL96435A0 (en)	1991-08-16
NO905086L (no)	1991-05-27
NO300065B1 (no)	1997-04-01
CN1052117A (zh)	1991-06-12
JPH03170487A (ja)	1991-07-24
CN1032754C (zh)	1996-09-11
CZ281422B6 (cs)	1996-09-11
ZM5390A1 (en)	1992-06-30
YU220890A (sh)	1992-12-21
PT95978B (pt)	1998-01-30
DE69022370D1 (de)	1995-10-19
CA2028756A1 (en)	1991-05-25
FI93459C (fi)	1995-04-10
AU630766B2 (en)	1992-11-05
HUT59414A (en)	1992-05-28
FI905788L (fi)	1991-05-25
HU206361B (en)	1992-10-28

Legal Events

Date	Code	Title	Description
1997-02-18	KB	Patent renewed
2001-07-24	MM9K	Patent not in force due to non-payment of renewal fees

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