OA10543A - Dérivés du 2-azabicyclo Ä2.2.1Ü heptane leur préparation et leur application - Google Patents

Dérivés du 2-azabicyclo Ä2.2.1Ü heptane leur préparation et leur application Download PDF

Info

Publication number: OA10543A
Authority: OA; OAPI
Prior art keywords: radical; general formula; product; carbon atoms; radicals
Prior art date: 1995-05-30

Application number

OA70143A

Other languages

English (en)

French (fr)

Inventor

Denis Largeau

Patrick Leon

Original Assignee

Rhone Poulenc Rorer Sa

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.)

1995-05-30

Filing date

1997-11-28

Publication date

2002-05-31

1995-05-30 Priority claimed from FR9506353A external-priority patent/FR2734822B1/fr

1997-11-28 Application filed by Rhone Poulenc Rorer Sa filed Critical Rhone Poulenc Rorer Sa

2002-05-31 Publication of OA10543A publication Critical patent/OA10543A/fr

Links

238000002360 preparation method Methods 0.000 title claims description 7
GYLMCBOAXJVARF-UHFFFAOYSA-N 3-azabicyclo[2.2.1]heptane Chemical class C1C2CCC1NC2 GYLMCBOAXJVARF-UHFFFAOYSA-N 0.000 title claims 4
-1 beta-naphthyl group Chemical group 0.000 claims abstract description 56
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 49
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 37
125000000217 alkyl group Chemical group 0.000 claims abstract description 13
238000005805 hydroxylation reaction Methods 0.000 claims abstract description 6
125000005843 halogen group Chemical group 0.000 claims abstract description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 3
150000003254 radicals Chemical group 0.000 claims description 51
125000006239 protecting group Chemical group 0.000 claims description 25
239000000203 mixture Substances 0.000 claims description 15
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 11
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 10
229910052799 carbon Inorganic materials 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 9
238000000034 method Methods 0.000 claims description 9
239000003960 organic solvent Substances 0.000 claims description 9
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 8
HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 claims description 7
229910052757 nitrogen Inorganic materials 0.000 claims description 7
125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
UFUASNAHBMBJIX-UHFFFAOYSA-N propan-1-one Chemical compound CC[C]=O UFUASNAHBMBJIX-UHFFFAOYSA-N 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 6
239000003054 catalyst Substances 0.000 claims description 6
238000007327 hydrogenolysis reaction Methods 0.000 claims description 6
LEVJVKGPFAQPOI-UHFFFAOYSA-N phenylmethanone Chemical compound O=[C]C1=CC=CC=C1 LEVJVKGPFAQPOI-UHFFFAOYSA-N 0.000 claims description 6
229910052783 alkali metal Inorganic materials 0.000 claims description 5
230000003647 oxidation Effects 0.000 claims description 5
238000007254 oxidation reaction Methods 0.000 claims description 5
230000001590 oxidative effect Effects 0.000 claims description 5
239000011541 reaction mixture Substances 0.000 claims description 5
LFTLOKWAGJYHHR-UHFFFAOYSA-N N-methylmorpholine N-oxide Chemical compound CN1(=O)CCOCC1 LFTLOKWAGJYHHR-UHFFFAOYSA-N 0.000 claims description 4
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 4
125000004429 atom Chemical group 0.000 claims description 4
229910052500 inorganic mineral Inorganic materials 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
239000011707 mineral Substances 0.000 claims description 4
239000007800 oxidant agent Substances 0.000 claims description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
125000004849 alkoxymethyl group Chemical group 0.000 claims description 3
239000002585 base Substances 0.000 claims description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
239000003153 chemical reaction reagent Substances 0.000 claims description 3
238000002425 crystallisation Methods 0.000 claims description 3
230000008025 crystallization Effects 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 3
LFMTUFVYMCDPGY-UHFFFAOYSA-N n,n-diethylethanamine oxide Chemical compound CC[N+]([O-])(CC)CC LFMTUFVYMCDPGY-UHFFFAOYSA-N 0.000 claims description 3
239000012285 osmium tetroxide Substances 0.000 claims description 3
229910000489 osmium tetroxide Inorganic materials 0.000 claims description 3
229910052763 palladium Inorganic materials 0.000 claims description 3
239000012286 potassium permanganate Substances 0.000 claims description 3
238000010992 reflux Methods 0.000 claims description 3
229910001925 ruthenium oxide Inorganic materials 0.000 claims description 3
WOCIAKWEIIZHES-UHFFFAOYSA-N ruthenium(iv) oxide Chemical compound O=[Ru]=O WOCIAKWEIIZHES-UHFFFAOYSA-N 0.000 claims description 3
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 2
238000006359 acetalization reaction Methods 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
230000032050 esterification Effects 0.000 claims description 2
238000005886 esterification reaction Methods 0.000 claims description 2
QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 claims description 2
125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 2
238000011065 in-situ storage Methods 0.000 claims description 2
150000002576 ketones Chemical class 0.000 claims description 2
150000003951 lactams Chemical class 0.000 claims description 2
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 2
230000001012 protector Effects 0.000 claims description 2
150000001721 carbon Chemical group 0.000 claims 6
238000004519 manufacturing process Methods 0.000 claims 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims 2
125000001931 aliphatic group Chemical group 0.000 claims 1
229910000102 alkali metal hydride Inorganic materials 0.000 claims 1
150000008046 alkali metal hydrides Chemical class 0.000 claims 1
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
239000003245 coal Substances 0.000 claims 1
ZFTFAPZRGNKQPU-UHFFFAOYSA-N dicarbonic acid Chemical compound OC(=O)OC(O)=O ZFTFAPZRGNKQPU-UHFFFAOYSA-N 0.000 claims 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims 1
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical class CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 abstract description 11
125000003545 alkoxy group Chemical group 0.000 abstract description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 3
125000001424 substituent group Chemical group 0.000 abstract description 2
OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 abstract 2
HREMGZQEPGHZNC-UHFFFAOYSA-N 2-cycloheptylazepane Chemical class C1CCCCCC1C1NCCCCC1 HREMGZQEPGHZNC-UHFFFAOYSA-N 0.000 abstract 1
239000002126 C01EB10 - Adenosine Substances 0.000 abstract 1
229960005305 adenosine Drugs 0.000 abstract 1
239000003795 chemical substances by application Substances 0.000 abstract 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 24
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
239000000243 solution Substances 0.000 description 15
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 12
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 8
238000001914 filtration Methods 0.000 description 7
238000003756 stirring Methods 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 6
125000004744 butyloxycarbonyl group Chemical group 0.000 description 6
238000001816 cooling Methods 0.000 description 6
239000000126 substance Substances 0.000 description 6
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 5
239000012074 organic phase Substances 0.000 description 5
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 4
ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 4
NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 4
JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 4
229910052938 sodium sulfate Inorganic materials 0.000 description 4
235000011152 sodium sulphate Nutrition 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
239000005708 Sodium hypochlorite Substances 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
238000010908 decantation Methods 0.000 description 3
238000001704 evaporation Methods 0.000 description 3
230000008020 evaporation Effects 0.000 description 3
CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 description 3
SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 3
HEWZVZIVELJPQZ-UHFFFAOYSA-N 2,2-dimethoxypropane Chemical compound COC(C)(C)OC HEWZVZIVELJPQZ-UHFFFAOYSA-N 0.000 description 2
ZFTGYVZYKWHOPY-UHFFFAOYSA-N 2-(1-phenylethyl)-2-azabicyclo[2.2.1]hept-5-ene Chemical compound C1C(C=C2)CC2N1C(C)C1=CC=CC=C1 ZFTGYVZYKWHOPY-UHFFFAOYSA-N 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
150000001241 acetals Chemical class 0.000 description 2
150000003973 alkyl amines Chemical class 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
239000003638 chemical reducing agent Substances 0.000 description 2
239000013078 crystal Substances 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
238000001035 drying Methods 0.000 description 2
JGJLWPGRMCADHB-UHFFFAOYSA-N hypobromite Chemical compound Br[O-] JGJLWPGRMCADHB-UHFFFAOYSA-N 0.000 description 2
WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
238000003760 magnetic stirring Methods 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000011591 potassium Substances 0.000 description 2
238000001228 spectrum Methods 0.000 description 2
239000007858 starting material Substances 0.000 description 2
JVCBVWTTXCNJBJ-UHFFFAOYSA-N 1-azabicyclo[2.2.1]heptane Chemical compound C1CC2CCN1C2 JVCBVWTTXCNJBJ-UHFFFAOYSA-N 0.000 description 1
RQEUFEKYXDPUSK-UHFFFAOYSA-N 1-phenylethylamine Chemical compound CC(N)C1=CC=CC=C1 RQEUFEKYXDPUSK-UHFFFAOYSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
208000024172 Cardiovascular disease Diseases 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 description 1
206010020772 Hypertension Diseases 0.000 description 1
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 1
DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 description 1
239000013543 active substance Substances 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 1
SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
125000002668 chloroacetyl group Chemical group ClCC(=O)* 0.000 description 1
230000003226 decolorizating effect Effects 0.000 description 1
125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
ODCCJTMPMUFERV-UHFFFAOYSA-N ditert-butyl carbonate Chemical compound CC(C)(C)OC(=O)OC(C)(C)C ODCCJTMPMUFERV-UHFFFAOYSA-N 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
MHYCRLGKOZWVEF-UHFFFAOYSA-N ethyl acetate;hydrate Chemical compound O.CCOC(C)=O MHYCRLGKOZWVEF-UHFFFAOYSA-N 0.000 description 1
125000006260 ethylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])C([H])([H])[H] 0.000 description 1
238000004128 high performance liquid chromatography Methods 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
239000010410 layer Substances 0.000 description 1
208000031225 myocardial ischemia Diseases 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
239000012044 organic layer Substances 0.000 description 1
229910052762 osmium Inorganic materials 0.000 description 1
SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 1
KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
239000002243 precursor Substances 0.000 description 1
OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
238000010926 purge Methods 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
150000003839 salts Chemical group 0.000 description 1
239000012047 saturated solution Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910000033 sodium borohydride Inorganic materials 0.000 description 1
239000012279 sodium borohydride Substances 0.000 description 1
XUXNAKZDHHEHPC-UHFFFAOYSA-M sodium bromate Chemical compound [Na+].[O-]Br(=O)=O XUXNAKZDHHEHPC-UHFFFAOYSA-M 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
XMVONEAAOPAGAO-UHFFFAOYSA-N sodium tungstate Chemical compound [Na+].[Na+].[O-][W]([O-])(=O)=O XMVONEAAOPAGAO-UHFFFAOYSA-N 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
125000004665 trialkylsilyl group Chemical group 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/52—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring condensed with a ring other than six-membered
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

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Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Saccharide Compounds (AREA)

OA70143A 1995-05-30 1997-11-28 Dérivés du 2-azabicyclo Ä2.2.1Ü heptane leur préparation et leur application OA10543A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR9506353A FR2734822B1 (fr)	1995-05-30	1995-05-30	Nouveaux derives du 2-azabicyclo(2.2.1)heptane, leur preparation et leur application

Publications (1)

Publication Number	Publication Date
OA10543A true OA10543A (fr)	2002-05-31

Family

ID=9479463

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
OA70143A OA10543A (fr)	1995-05-30	1997-11-28	Dérivés du 2-azabicyclo Ä2.2.1Ü heptane leur préparation et leur application

Country Status (25)

Country	Link
EP (1)	EP0828740B1 (de)
JP (2)	JP4097287B2 (de)
KR (1)	KR100488393B1 (de)
CN (1)	CN1249034C (de)
AP (1)	AP973A (de)
AT (1)	ATE205210T1 (de)
AU (1)	AU711057B2 (de)
BG (1)	BG63084B1 (de)
BR (1)	BR9608513A (de)
CA (1)	CA2219456A1 (de)
CZ (1)	CZ286483B6 (de)
DE (1)	DE69615020T2 (de)
DK (1)	DK0828740T3 (de)
EA (1)	EA000963B1 (de)
ES (1)	ES2163023T3 (de)
GR (1)	GR3036536T3 (de)
HU (1)	HUP9900787A3 (de)
NO (1)	NO311431B1 (de)
OA (1)	OA10543A (de)
PL (1)	PL186195B1 (de)
PT (1)	PT828740E (de)
RO (1)	RO119414B1 (de)
SI (1)	SI0828740T1 (de)
SK (1)	SK283809B6 (de)
UA (1)	UA64695C2 (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0719719A (ja) *	1993-07-05	1995-01-20	Matsushita Electric Ind Co Ltd	断熱箱体

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4954504A (en) *	1986-11-14	1990-09-04	Ciba-Geigy Corporation	N9 -cyclopentyl-substituted adenine derivatives having adenosine-2 receptor stimulating activity
US5063233A (en) *	1986-11-14	1991-11-05	Ciba-Geigy Corporation	N9 -cyclopentyl-substituted adenine derivatives useful as adenosine receptor agonists
US4803272A (en) *	1987-02-24	1989-02-07	E. I. Du Pont De Nemours And Company	S-modified adenosyl-1,8-diamino-3-thiooctane derivatives
US5561134A (en) *	1990-09-25	1996-10-01	Rhone-Poulenc Rorer Pharmaceuticals Inc.	Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties
GB9301000D0 (en) *	1993-01-20	1993-03-10	Glaxo Group Ltd	Chemical compounds

1996
- 1996-05-28 SK SK1612-97A patent/SK283809B6/sk not_active IP Right Cessation
- 1996-05-28 CZ CZ19973777A patent/CZ286483B6/cs not_active IP Right Cessation
- 1996-05-28 AP APAP/P/1997/001149A patent/AP973A/en active
- 1996-05-28 ES ES96917555T patent/ES2163023T3/es not_active Expired - Lifetime
- 1996-05-28 PL PL96323680A patent/PL186195B1/pl not_active IP Right Cessation
- 1996-05-28 AT AT96917555T patent/ATE205210T1/de active
- 1996-05-28 EP EP96917555A patent/EP0828740B1/de not_active Expired - Lifetime
- 1996-05-28 KR KR1019970708582A patent/KR100488393B1/ko not_active Expired - Fee Related
- 1996-05-28 HU HU9900787A patent/HUP9900787A3/hu unknown
- 1996-05-28 CA CA002219456A patent/CA2219456A1/fr not_active Abandoned
- 1996-05-28 EA EA199700440A patent/EA000963B1/ru not_active IP Right Cessation
- 1996-05-28 AU AU60087/96A patent/AU711057B2/en not_active Ceased
- 1996-05-28 DK DK96917555T patent/DK0828740T3/da active
- 1996-05-28 DE DE69615020T patent/DE69615020T2/de not_active Expired - Lifetime
- 1996-05-28 SI SI9630340T patent/SI0828740T1/xx unknown
- 1996-05-28 PT PT96917555T patent/PT828740E/pt unknown
- 1996-05-28 UA UA97115616A patent/UA64695C2/uk unknown
- 1996-05-28 BR BR9608513A patent/BR9608513A/pt not_active IP Right Cessation
- 1996-05-28 RO RO97-02201A patent/RO119414B1/ro unknown
- 1996-05-28 JP JP53624696A patent/JP4097287B2/ja not_active Expired - Fee Related
1997
- 1997-11-28 BG BG102081A patent/BG63084B1/bg unknown
- 1997-11-28 NO NO19975487A patent/NO311431B1/no not_active IP Right Cessation
- 1997-11-28 OA OA70143A patent/OA10543A/fr unknown
2001
- 2001-09-06 GR GR20010400676T patent/GR3036536T3/el unknown
2002
- 2002-02-20 CN CNB021046816A patent/CN1249034C/zh not_active Expired - Fee Related
2007
- 2007-07-09 JP JP2007179423A patent/JP2007262089A/ja active Pending

Also Published As

Publication number	Publication date
BG63084B1 (bg)	2001-03-30
PT828740E (pt)	2002-02-28
CN1397549A (zh)	2003-02-19
SK283809B6 (sk)	2004-02-03
NO975487L (no)	1997-11-28
EA000963B1 (ru)	2000-08-28
DE69615020T2 (de)	2002-03-21
DK0828740T3 (da)	2002-12-02
AU711057B2 (en)	1999-10-07
CZ286483B6 (en)	2000-04-12
EP0828740B1 (de)	2001-09-05
PL186195B1 (pl)	2003-11-28
CN1249034C (zh)	2006-04-05
DE69615020D1 (de)	2001-10-11
EP0828740A1 (de)	1998-03-18
GR3036536T3 (en)	2001-12-31
JP2007262089A (ja)	2007-10-11
AP9701149A0 (en)	1998-01-31
JPH11505861A (ja)	1999-05-25
AP973A (en)	2001-06-08
JP4097287B2 (ja)	2008-06-11
CA2219456A1 (fr)	1996-12-05
PL323680A1 (en)	1998-04-14
NO975487D0 (no)	1997-11-28
UA64695C2 (en)	2004-03-15
KR19990022103A (ko)	1999-03-25
ATE205210T1 (de)	2001-09-15
NO311431B1 (no)	2001-11-26
MX9708995A (es)	1998-03-31
ES2163023T3 (es)	2002-01-16
EA199700440A1 (ru)	1998-08-27
KR100488393B1 (ko)	2005-08-30
BR9608513A (pt)	1999-02-02
RO119414B1 (ro)	2004-10-29
HUP9900787A2 (hu)	1999-07-28
CZ377797A3 (cs)	1998-03-18
BG102081A (en)	1998-11-30
SI0828740T1 (en)	2001-12-31
AU6008796A (en)	1996-12-18
SK161297A3 (en)	1998-04-08
HUP9900787A3 (en)	2001-05-28

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EP0586471B1 (de)	1994-12-28	Perhydroisoindol derivate und ihre herstellung
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WO1991017976A1 (fr)	1991-11-28	Procede de preparation enantioselective de derives de la phenylisoserine
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EP1268397B1 (de)	2007-12-05	Verfahren zur herstellung von (2s,3r,4s)-4-hydroxyisoleucin und analoga
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EP0635002B1 (de)	1998-07-22	Neue perhydroisoindolderivate und ihre herstellung
WO1996038447A1 (fr)	1996-12-05	Derives du 2-azabicyclo[2.2.1]heptane, leur preparation et leur application
OA10543A (fr)	2002-05-31	Dérivés du 2-azabicyclo Ä2.2.1Ü heptane leur préparation et leur application
CH638183A5 (fr)	1983-09-15	Derives de pyrrolidine et de piperidine.
US5670649A (en)	1997-09-23	Derivatives of 2-azabicyclo 2.2.1!heptane, their preparation and their application
WO2004083237A1 (fr)	2004-09-30	NOUVEAU PROCEDE DE SYNTHESE DE L’ACIDE (2S, 3aS, 7aS)-PERHYDROINDOLE-2-CARBOXYLIQUE ET DE SES ESTERS, ET APPLICATION A LA SYNTHESE DU PERINDOPRIL
EP1362845B1 (de)	2009-10-14	Neues Verfahren zur Herstellung von Estern des N-((S)-1-Carboxybutyl)-(S)-alanins und seine Verwendung in der Synthese von Perindopril
EP1400531B1 (de)	2006-01-04	Verfahren zur Herstellung von N-((S)-1-(Etoxycarbonyl)butyl)-(S)-alanin und Verwendung in der Synthese von Perindopril
WO2005030719A1 (fr)	2005-04-07	Nouveau procede de preparation du cis-octahydro-isoindole
MXPA97008995A (en)	1998-10-15	New derivatives of 2-azabiciclo [2.2.1] heptano, its preparation and its application
FR2777888A1 (fr)	1999-10-29	Nouveaux derives de l'acide (3,4,7,8,9,10-hexahydro-6,10- dioxo-6h-pyridazino[1,2-a][1,2]diazepine-1-carboxylique, leur procede de preparation et leur application a la preparation de medicaments
WO2000015617A1 (fr)	2000-03-23	Derives de 2-aminoethyl-quinoleine, leur preparation et leur application en therapeutique
FR2737208A1 (fr)	1997-01-31	Nouvelles fluorovindolines, precurseurs d'analogues de la vinblastine et de la vinorelbine,leurs procedes de preparation et leur utilisation comme medicament
CH671763A5 (de)	1989-09-29