SU406360A1 - - Google Patents

Info

Publication number: SU406360A1
Authority: SU; USSR - Soviet Union
Prior art keywords: phenyl; dihydro; chloro; benzodiazepin; methyl
Prior art date

Application number

SU2255A

Other languages

English (en)

Russian (ru)

Other versions

SU404253A1 (2

SU406359A1 (2

SU402219A1 (ru

SU58868A1 (ru

Inventor

Армии Вальзер Швейцари Иностранцы Йозеф Геллербах

Original Assignee

Иностранна фирма Ф. Гофманн Рош Швейцари

Publication of SU406360A1 publication Critical patent/SU406360A1/ru

Publication of SU404253A1 publication Critical patent/SU404253A1/ru

Publication of SU406359A1 publication Critical patent/SU406359A1/ru

Publication of SU402219A1 publication Critical patent/SU402219A1/ru

1940-06-11 Application filed by Иностранна фирма Ф. Гофманн Рош Швейцари filed Critical Иностранна фирма Ф. Гофманн Рош Швейцари

1940-06-11 Priority to SU2255A priority Critical patent/SU58868A1/ru

1940-06-11 Priority claimed from SU2255A external-priority patent/SU58868A1/ru

1940-11-30 Application granted granted Critical

1940-11-30 Publication of SU58868A1 publication Critical patent/SU58868A1/ru

Links

YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 28
-1 acychoxyalkyl Chemical group 0.000 description 22
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
150000001875 compounds Chemical class 0.000 description 15
239000000203 mixture Substances 0.000 description 15
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 7
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
125000003545 alkoxy group Chemical group 0.000 description 6
125000005843 halogen group Chemical group 0.000 description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
238000000034 method Methods 0.000 description 6
239000003960 organic solvent Substances 0.000 description 6
150000003839 salts Chemical class 0.000 description 6
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 5
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
239000002585 base Substances 0.000 description 5
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
125000004390 alkyl sulfonyl group Chemical group 0.000 description 4
150000002170 ethers Chemical class 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
125000004438 haloalkoxy group Chemical group 0.000 description 4
125000001188 haloalkyl group Chemical group 0.000 description 4
150000002430 hydrocarbons Chemical group 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
235000011121 sodium hydroxide Nutrition 0.000 description 4
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
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 3
125000001931 aliphatic group Chemical group 0.000 description 3
229910052783 alkali metal Inorganic materials 0.000 description 3
150000008044 alkali metal hydroxides Chemical class 0.000 description 3
125000005083 alkoxyalkoxy group Chemical group 0.000 description 3
229930195733 hydrocarbon Natural products 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000005041 acyloxyalkyl group Chemical group 0.000 description 2
239000003513 alkali Substances 0.000 description 2
150000001340 alkali metals Chemical class 0.000 description 2
125000004644 alkyl sulfinyl group Chemical group 0.000 description 2
125000004414 alkyl thio group Chemical group 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
238000002425 crystallisation Methods 0.000 description 2
230000008025 crystallization Effects 0.000 description 2
125000004985 dialkyl amino alkyl group Chemical group 0.000 description 2
125000004663 dialkyl amino group Chemical group 0.000 description 2
NPOMSUOUAZCMBL-UHFFFAOYSA-N dichloromethane;ethoxyethane Chemical compound ClCCl.CCOCC NPOMSUOUAZCMBL-UHFFFAOYSA-N 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
ZKQFHRVKCYFVCN-UHFFFAOYSA-N ethoxyethane;hexane Chemical compound CCOCC.CCCCCC ZKQFHRVKCYFVCN-UHFFFAOYSA-N 0.000 description 2
OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 2
150000008282 halocarbons Chemical class 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
125000005059 halophenyl group Chemical group 0.000 description 2
230000007062 hydrolysis Effects 0.000 description 2
238000006460 hydrolysis reaction Methods 0.000 description 2
238000002955 isolation Methods 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
239000012071 phase Substances 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
125000004076 pyridyl group Chemical group 0.000 description 2
238000010992 reflux Methods 0.000 description 2
239000000052 vinegar Substances 0.000 description 2
RGGLEJFUEMKQSH-UHFFFAOYSA-N 1,4-benzodiazepin-2-one Chemical compound O=C1C=NC=C2C=CC=CC2=N1 RGGLEJFUEMKQSH-UHFFFAOYSA-N 0.000 description 1
125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 1
YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
NDJGAFQWMURJLX-UHFFFAOYSA-N 7-chloro-5-(2-chlorophenyl)-1-(methoxymethyl)-3h-1,4-benzodiazepin-2-one Chemical compound N=1CC(=O)N(COC)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1Cl NDJGAFQWMURJLX-UHFFFAOYSA-N 0.000 description 1
IFTYELQPJWAOCM-UHFFFAOYSA-N 7-nitro-5-phenyl-1-(propoxymethyl)-3H-1,4-benzodiazepin-2-one Chemical compound [N+](=O)([O-])C=1C=CC2=C(C(=NCC(N2COCCC)=O)C2=CC=CC=C2)C1 IFTYELQPJWAOCM-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
VAWZJOADXFNURD-UHFFFAOYSA-N CC(C1=O)N=C(C2=CC=CC=C2)C(C=C(C=C2)Cl)=C2N1OCCCl Chemical compound CC(C1=O)N=C(C2=CC=CC=C2)C(C=C(C=C2)Cl)=C2N1OCCCl VAWZJOADXFNURD-UHFFFAOYSA-N 0.000 description 1
HMDOVKQLJVULLJ-UHFFFAOYSA-N CC1C(=O)N(C2=C(C=C(C=C2)Cl)C(=N1)C3=CC=CC=C3)SC Chemical compound CC1C(=O)N(C2=C(C=C(C=C2)Cl)C(=N1)C3=CC=CC=C3)SC HMDOVKQLJVULLJ-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
238000006136 alcoholysis reaction Methods 0.000 description 1
229910000102 alkali metal hydride Inorganic materials 0.000 description 1
150000008046 alkali metal hydrides Chemical class 0.000 description 1
125000002431 aminoalkoxy group Chemical group 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
125000003435 aroyl group Chemical group 0.000 description 1
229940053197 benzodiazepine derivative antiepileptics Drugs 0.000 description 1
150000001557 benzodiazepines Chemical class 0.000 description 1
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
HRQGCQVOJVTVLU-UHFFFAOYSA-N bis(chloromethyl) ether Chemical compound ClCOCCl HRQGCQVOJVTVLU-UHFFFAOYSA-N 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
125000006309 butyl amino group Chemical group 0.000 description 1
125000001589 carboacyl group Chemical group 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
125000002668 chloroacetyl group Chemical group ClCC(=O)* 0.000 description 1
238000011097 chromatography purification Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
238000006114 decarboxylation reaction Methods 0.000 description 1
125000005265 dialkylamine group Chemical group 0.000 description 1
125000004984 dialkylaminoalkoxy group Chemical group 0.000 description 1
WGLUMOCWFMKWIL-UHFFFAOYSA-N dichloromethane;methanol Chemical compound OC.ClCCl WGLUMOCWFMKWIL-UHFFFAOYSA-N 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
SRCZQMGIVIYBBJ-UHFFFAOYSA-N ethoxyethane;ethyl acetate Chemical compound CCOCC.CCOC(C)=O SRCZQMGIVIYBBJ-UHFFFAOYSA-N 0.000 description 1
HWJHWSBFPPPIPD-UHFFFAOYSA-N ethoxyethane;propan-2-one Chemical compound CC(C)=O.CCOCC HWJHWSBFPPPIPD-UHFFFAOYSA-N 0.000 description 1
125000004494 ethyl ester group Chemical group 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
239000012634 fragment Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
125000001475 halogen functional group Chemical group 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
150000004678 hydrides Chemical class 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
125000005113 hydroxyalkoxy group Chemical group 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000001819 mass spectrum Methods 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
150000007530 organic bases Chemical group 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
125000005824 oxyalkoxy group Chemical group 0.000 description 1
125000005429 oxyalkyl group Chemical group 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
125000005489 p-toluenesulfonic acid group Chemical class 0.000 description 1
230000020477 pH reduction Effects 0.000 description 1
150000004965 peroxy acids Chemical class 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
229910000104 sodium hydride Inorganic materials 0.000 description 1
239000012312 sodium hydride Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000000725 suspension Substances 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1

SU2255A 1940-06-11 1940-06-11 Ламповый генератор SU58868A1 (ru)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
SU2255A SU58868A1 (ru)	1940-06-11	1940-06-11	Ламповый генератор

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SU2255A SU58868A1 (ru)	1940-06-11	1940-06-11	Ламповый генератор

Publications (5)

Publication Number	Publication Date
SU406360A1 true SU406360A1 (2)
SU404253A1 SU404253A1 (2)
SU406359A1 SU406359A1 (2)
SU402219A1 SU402219A1 (ru)
SU58868A1 SU58868A1 (ru)	1940-11-30

Family

ID=48241128

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU2255A SU58868A1 (ru)	1940-06-11	1940-06-11	Ламповый генератор

Country Status (1)

Country	Link
SU (1)	SU58868A1 (2)

1940
- 1940-06-11 SU SU2255A patent/SU58868A1/ru active

Publication	Publication Date	Title
EP0138280A2 (en)	1985-04-24	Blood-pressure lowering piperazine derivatives
NO841106L (no)	1984-09-24	Fremgangsmaate for fremstilling av kondenserte imidazolderivater
JPH0317071A (ja)	1991-01-25	３―アミノ―５―アミノカルボニル―１，２，４―トリアゾール誘導体類の製造方法
SE500669C2 (sv)	1994-08-08	Bensimidazolderivat
EP0554829A2 (en)	1993-08-11	Pyrazole derivatives with antiinflammatory, analgesic and antithrombolic activity
MXPA06011130A (es)	2007-01-25	Proceso para producir un compuesto de 5 - hidroxi - 4 - tiometilpirazol.
JPH0774208B2 (ja)	1995-08-09	新規なベンズオキサジン誘導体及びその中間体並びにその医薬
FI65066C (fi)	1984-03-12	Foerfarande foer framstaellning av nya terapeutiskt verksamma 2-merkaptoimidazolderivat
US3770734A (en)	1973-11-06	3-oxo-2,3-dihydro-1,4-benzoxazine derivatives
NO162414B (no)	1989-09-18	Fleksibel beholder for transport og lagring av massegods.
SU406360A1 (2)
SK161499A3 (en)	2000-06-12	Process for producing isooxazolidinedione compound
EA003468B1 (ru)	2003-06-26	Способ получения производных морфолина
FI89267B (fi)	1993-05-31	Foerfarande foer framstaellning av terapeutiskt aktiva 4,5-dihydro-oxazoler
JPH02145584A (ja)	1990-06-05	クロマン誘導体
US5968967A (en)	1999-10-19	Pyrazolones derivatives
US3784542A (en)	1974-01-08	Benzodiazepin-2-ones
SU453841A3 (ru)	1974-12-15	Способ получения производных бензодиазепина
US4950764A (en)	1990-08-21	2-aryl-4-isoxazolin-3-one derivatives
US3882139A (en)	1975-05-06	2-{8 3-(Hydroxymethyl)-5-(phthalimidomethyl)-4H,1,2,4-triazol-4-yl{9 benzophenones
SU404253A1 (2)
US3732211A (en)	1973-05-08	1-acyloxyether-1,4-benzodiazepin-2-ones and methods for their preparation
GB2059960A (en)	1981-04-29	Method for producing penicillanic acid derivatives
US3879413A (en)	1975-04-22	Process for the production of 6-phenyl-4-H-s-triazolo {8 4,3-a{9 {8 1,4{9 benzodiazepines
SU406359A1 (2)