IL120968A - Production process - N - (α - D - methyl - ß - noble theopropionyl) Proline - Google Patents
Production process - N - (α - D - methyl - ß - noble theopropionyl) ProlineInfo
- Publication number
- IL120968A IL120968A IL12096896A IL12096896A IL120968A IL 120968 A IL120968 A IL 120968A IL 12096896 A IL12096896 A IL 12096896A IL 12096896 A IL12096896 A IL 12096896A IL 120968 A IL120968 A IL 120968A
- Authority
- IL
- Israel
- Prior art keywords
- methyl
- proline
- reaction
- schotten
- formula
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 58
- 229960002429 proline Drugs 0.000 claims description 227
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 98
- 150000001875 compounds Chemical class 0.000 claims description 80
- 239000002253 acid Substances 0.000 claims description 73
- 238000003436 Schotten-Baumann reaction Methods 0.000 claims description 69
- 238000006243 chemical reaction Methods 0.000 claims description 69
- 150000004820 halides Chemical class 0.000 claims description 64
- 229910052799 carbon Inorganic materials 0.000 claims description 62
- 238000002425 crystallisation Methods 0.000 claims description 53
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 claims description 52
- 230000008025 crystallization Effects 0.000 claims description 50
- 239000012736 aqueous medium Substances 0.000 claims description 49
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 49
- 238000011282 treatment Methods 0.000 claims description 44
- 229910001868 water Inorganic materials 0.000 claims description 40
- 229930182821 L-proline Natural products 0.000 claims description 39
- 238000005947 deacylation reaction Methods 0.000 claims description 37
- 239000012535 impurity Substances 0.000 claims description 37
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 36
- 239000002243 precursor Substances 0.000 claims description 35
- 238000003756 stirring Methods 0.000 claims description 33
- 230000015572 biosynthetic process Effects 0.000 claims description 32
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 31
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 claims description 24
- 239000003795 chemical substances by application Substances 0.000 claims description 19
- 230000020176 deacylation Effects 0.000 claims description 18
- 239000000126 substance Substances 0.000 claims description 18
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims description 16
- 235000015497 potassium bicarbonate Nutrition 0.000 claims description 16
- 239000011736 potassium bicarbonate Substances 0.000 claims description 16
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims description 16
- 229940086066 potassium hydrogencarbonate Drugs 0.000 claims description 16
- 239000003960 organic solvent Substances 0.000 claims description 13
- 239000003513 alkali Substances 0.000 claims description 8
- 230000002378 acidificating effect Effects 0.000 claims description 7
- -1 thiopropionic acid halide Chemical class 0.000 claims description 7
- 238000002955 isolation Methods 0.000 claims description 6
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 4
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 230000003287 optical effect Effects 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims 1
- 230000015654 memory Effects 0.000 abstract 2
- FAKRSMQSSFJEIM-RQJHMYQMSA-N captopril Chemical compound SC[C@@H](C)C(=O)N1CCC[C@H]1C(O)=O FAKRSMQSSFJEIM-RQJHMYQMSA-N 0.000 description 73
- 229960000830 captopril Drugs 0.000 description 73
- 239000013078 crystal Substances 0.000 description 67
- 239000011541 reaction mixture Substances 0.000 description 45
- 239000000203 mixture Substances 0.000 description 42
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 40
- 239000007864 aqueous solution Substances 0.000 description 40
- 239000000243 solution Substances 0.000 description 38
- 238000013019 agitation Methods 0.000 description 37
- 239000006227 byproduct Substances 0.000 description 31
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 30
- 239000000047 product Substances 0.000 description 28
- 239000008367 deionised water Substances 0.000 description 20
- 229910021641 deionized water Inorganic materials 0.000 description 20
- 239000002002 slurry Substances 0.000 description 19
- 229910052757 nitrogen Inorganic materials 0.000 description 16
- GNMSLDIYJOSUSW-LURJTMIESA-N N-acetyl-L-proline Chemical compound CC(=O)N1CCC[C@H]1C(O)=O GNMSLDIYJOSUSW-LURJTMIESA-N 0.000 description 14
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 11
- 238000001914 filtration Methods 0.000 description 11
- 235000011118 potassium hydroxide Nutrition 0.000 description 11
- 229940093932 potassium hydroxide Drugs 0.000 description 11
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 10
- 239000000706 filtrate Substances 0.000 description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 239000002585 base Substances 0.000 description 8
- 238000001816 cooling Methods 0.000 description 8
- 229910001873 dinitrogen Inorganic materials 0.000 description 8
- 238000004128 high performance liquid chromatography Methods 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 7
- 230000008030 elimination Effects 0.000 description 7
- 238000003379 elimination reaction Methods 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-UHFFFAOYSA-N 0.000 description 5
- 150000007529 inorganic bases Chemical class 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000012299 nitrogen atmosphere Substances 0.000 description 5
- 239000011780 sodium chloride Substances 0.000 description 5
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 4
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 4
- 229910052808 lithium carbonate Inorganic materials 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000007935 neutral effect Effects 0.000 description 4
- 150000007530 organic bases Chemical class 0.000 description 4
- 230000020477 pH reduction Effects 0.000 description 4
- 229910000027 potassium carbonate Inorganic materials 0.000 description 4
- 235000011181 potassium carbonates Nutrition 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- 241000894007 species Species 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- MHRDCHHESNJQIS-UHFFFAOYSA-N 2-methyl-3-sulfanylpropanoic acid Chemical compound SCC(C)C(O)=O MHRDCHHESNJQIS-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 229960001413 acetanilide Drugs 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 239000013256 coordination polymer Substances 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 238000007710 freezing Methods 0.000 description 3
- 230000008014 freezing Effects 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 230000009965 odorless effect Effects 0.000 description 3
- 238000010979 pH adjustment Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000007086 side reaction Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 150000001722 carbon compounds Chemical class 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000007810 chemical reaction solvent Substances 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- 229910017053 inorganic salt Inorganic materials 0.000 description 2
- 229910000032 lithium hydrogen carbonate Inorganic materials 0.000 description 2
- HQRPHMAXFVUBJX-UHFFFAOYSA-M lithium;hydrogen carbonate Chemical compound [Li+].OC([O-])=O HQRPHMAXFVUBJX-UHFFFAOYSA-M 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- UUUHXMGGBIUAPW-UHFFFAOYSA-N 1-[1-[2-[[5-amino-2-[[1-[5-(diaminomethylideneamino)-2-[[1-[3-(1h-indol-3-yl)-2-[(5-oxopyrrolidine-2-carbonyl)amino]propanoyl]pyrrolidine-2-carbonyl]amino]pentanoyl]pyrrolidine-2-carbonyl]amino]-5-oxopentanoyl]amino]-3-methylpentanoyl]pyrrolidine-2-carbon Chemical compound C1CCC(C(=O)N2C(CCC2)C(O)=O)N1C(=O)C(C(C)CC)NC(=O)C(CCC(N)=O)NC(=O)C1CCCN1C(=O)C(CCCN=C(N)N)NC(=O)C1CCCN1C(=O)C(CC=1C2=CC=CC=C2NC=1)NC(=O)C1CCC(=O)N1 UUUHXMGGBIUAPW-UHFFFAOYSA-N 0.000 description 1
- PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 102000004270 Peptidyl-Dipeptidase A Human genes 0.000 description 1
- 108090000882 Peptidyl-Dipeptidase A Proteins 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229940030600 antihypertensive agent Drugs 0.000 description 1
- 239000002220 antihypertensive agent Substances 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
- 238000009835 boiling Methods 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- ZWKRXBCJAUKDCI-KRCVMZOZSA-N captopril disulfide Chemical compound O=C([C@H](C)CSSCC(C)C(=O)N1[C@@H](CCC1)C(O)=O)N1CCC[C@H]1C(O)=O ZWKRXBCJAUKDCI-KRCVMZOZSA-N 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000003381 deacetylation reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000012851 eutrophication Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000003168 generic drug Substances 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- XIXYJCCQFKSBHG-UHFFFAOYSA-L lithium sodium hydrogen carbonate Chemical compound C([O-])([O-])=O.[Na+].C(O)(O)=O.[Li+] XIXYJCCQFKSBHG-UHFFFAOYSA-L 0.000 description 1
- RFROGNZGWFLDEB-UHFFFAOYSA-L lithium sodium hydrogen carbonate hydroxide Chemical compound C([O-])(O)=O.[Na+].[OH-].[Li+] RFROGNZGWFLDEB-UHFFFAOYSA-L 0.000 description 1
- INHCSSUBVCNVSK-UHFFFAOYSA-L lithium sulfate Inorganic materials [Li+].[Li+].[O-]S([O-])(=O)=O INHCSSUBVCNVSK-UHFFFAOYSA-L 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 229960003975 potassium Drugs 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000008057 potassium phosphate buffer Substances 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- RBTVSNLYYIMMKS-UHFFFAOYSA-N tert-butyl 3-aminoazetidine-1-carboxylate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)N1CC(N)C1 RBTVSNLYYIMMKS-UHFFFAOYSA-N 0.000 description 1
- HFRXJVQOXRXOPP-UHFFFAOYSA-N thionyl bromide Chemical compound BrS(Br)=O HFRXJVQOXRXOPP-UHFFFAOYSA-N 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyrrole Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IL13080596A IL130805A0 (en) | 1995-10-06 | 1996-10-07 | Process for producing n-(d-alpha-methyl-beta-mercaptopropionyl)-l-proline and intermediates thereof |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28688695 | 1995-10-06 | ||
| JP8122727A JPH09157251A (ja) | 1995-10-06 | 1996-04-19 | Ｎ−（Ｄ−α−メチル−β−メルカプトプロピオニル）−Ｌ−プロリン及び該中間体の製造方法 |
| PCT/JP1996/002902 WO1997012858A1 (fr) | 1995-10-06 | 1996-10-07 | PROCEDE DE PRODUCTION DE N-(D-α-METHYLE-β-MERCAPTOPROPIONYLE)-L-PROLINE ET DE SES INTERMEDIAIRES |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL120968A0 IL120968A0 (en) | 1997-11-20 |
| IL120968A true IL120968A (en) | 2002-09-12 |
Family
ID=26459801
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL12096896A IL120968A (en) | 1995-10-06 | 1996-10-07 | Production process - N - (α - D - methyl - ß - noble theopropionyl) Proline |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US5917055A (tr) |
| EP (1) | EP0802182B1 (tr) |
| JP (1) | JPH09157251A (tr) |
| AT (1) | ATE248144T1 (tr) |
| CA (1) | CA2206396A1 (tr) |
| DE (1) | DE69629661T2 (tr) |
| ES (1) | ES2206593T3 (tr) |
| HR (1) | HRP960449A2 (tr) |
| HU (1) | HUP9801362A3 (tr) |
| IL (1) | IL120968A (tr) |
| IN (1) | IN182217B (tr) |
| SI (1) | SI9620018A (tr) |
| WO (1) | WO1997012858A1 (tr) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3980684B2 (ja) | 1996-10-11 | 2007-09-26 | 株式会社カネカ | 高品質カプトプリルの簡便な製造方法 |
| PT915088E (pt) | 1997-10-31 | 2003-01-31 | Hoffmann La Roche | Derivados de d-prolina |
| EP1746503A1 (en) | 2005-07-12 | 2007-01-24 | Mitel Networks Corporation | Dynamic mailbox size configuraration by self-modification based on historical behavior |
| DE102005055811A1 (de) | 2005-11-23 | 2007-05-31 | Novaliq Gmbh | Verwendung einer Zusammensetzung zur Konservierung von Organen und Gliedmaßen |
| WO2018202835A1 (en) | 2017-05-05 | 2018-11-08 | Novaliq Gmbh | Process for the production of semifluorinated alkanes |
| CN110146624B (zh) * | 2019-06-14 | 2022-02-22 | 湖南汉森制药股份有限公司 | 一种卡托普利有关物质的检测方法 |
| CN117693498A (zh) * | 2021-07-13 | 2024-03-12 | 香港大学 | Ros响应性卡托普利-肉桂醛前药及其组合物和方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6345252A (ja) * | 1987-03-18 | 1988-02-26 | Chugai Pharmaceut Co Ltd | プロリン誘導体 |
| JP2896818B2 (ja) * | 1991-04-02 | 1999-05-31 | 三菱レイヨン株式会社 | Ｌ−プロリン誘導体の製造法 |
| JPH05221966A (ja) * | 1992-02-18 | 1993-08-31 | Mitsubishi Rayon Co Ltd | Ｌ−プロリン誘導体の製造方法 |
| JPH0680628A (ja) * | 1992-07-14 | 1994-03-22 | Mitsubishi Rayon Co Ltd | Ｎ−（Ｄ−α−アルキル−β−メルカプトプロピオニル）−Ｌ−プロリンの精製法 |
| JPH0710835A (ja) * | 1993-06-25 | 1995-01-13 | Kyowa Hakko Kogyo Co Ltd | Ｌ−プロリン誘導体の精製法 |
| US5387697A (en) * | 1994-06-13 | 1995-02-07 | Merck & Co., Inc. | Process for the preparation of 1-[3-acetylthio-2(s)-methylpropanoyl]-l-proline |
-
1996
- 1996-04-19 JP JP8122727A patent/JPH09157251A/ja active Pending
- 1996-10-03 HR HR8-122727A patent/HRP960449A2/hr not_active Application Discontinuation
- 1996-10-04 IN IN1754CA1996 patent/IN182217B/en unknown
- 1996-10-07 CA CA002206396A patent/CA2206396A1/en not_active Abandoned
- 1996-10-07 ES ES96932825T patent/ES2206593T3/es not_active Expired - Lifetime
- 1996-10-07 EP EP96932825A patent/EP0802182B1/en not_active Expired - Lifetime
- 1996-10-07 HU HU9801362A patent/HUP9801362A3/hu unknown
- 1996-10-07 DE DE69629661T patent/DE69629661T2/de not_active Expired - Fee Related
- 1996-10-07 AT AT96932825T patent/ATE248144T1/de not_active IP Right Cessation
- 1996-10-07 WO PCT/JP1996/002902 patent/WO1997012858A1/ja not_active Application Discontinuation
- 1996-10-07 IL IL12096896A patent/IL120968A/en not_active IP Right Cessation
- 1996-10-07 SI SI9620018A patent/SI9620018A/sl not_active IP Right Cessation
- 1996-10-07 US US08/849,337 patent/US5917055A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| HUP9801362A3 (en) | 1998-12-28 |
| ATE248144T1 (de) | 2003-09-15 |
| EP0802182B1 (en) | 2003-08-27 |
| DE69629661D1 (de) | 2003-10-02 |
| CA2206396A1 (en) | 1997-04-10 |
| ES2206593T3 (es) | 2004-05-16 |
| HUP9801362A2 (hu) | 1998-09-28 |
| SI9620018A (en) | 1997-12-31 |
| JPH09157251A (ja) | 1997-06-17 |
| US5917055A (en) | 1999-06-29 |
| WO1997012858A1 (fr) | 1997-04-10 |
| DE69629661T2 (de) | 2004-06-24 |
| IL120968A0 (en) | 1997-11-20 |
| HRP960449A2 (en) | 1998-02-28 |
| EP0802182A1 (en) | 1997-10-22 |
| EP0802182A4 (en) | 2001-01-17 |
| IN182217B (tr) | 1999-02-06 |
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| Date | Code | Title | Description |
|---|---|---|---|
| FF | Patent granted | ||
| KB | Patent renewed | ||
| MM9K | Patent not in force due to non-payment of renewal fees |