NO317356B1 - 4,10beta-diacetoksy-2alfa-benzoyloksy-5beta,20-epoksy-1-hydroksy-9-okso-19-nor-cyklopropa[G]tax-11-en-13<alfa>-yl (2R,3S)-3-tert-butoksykarbonylamino-2-hydroksy-3-fenylpropionat dihydrat, samt fremstilling derav - Google Patents
4,10beta-diacetoksy-2alfa-benzoyloksy-5beta,20-epoksy-1-hydroksy-9-okso-19-nor-cyklopropa[G]tax-11-en-13<alfa>-yl (2R,3S)-3-tert-butoksykarbonylamino-2-hydroksy-3-fenylpropionat dihydrat, samt fremstilling derav Download PDFInfo
- Publication number
- NO317356B1 NO317356B1 NO19982561A NO982561A NO317356B1 NO 317356 B1 NO317356 B1 NO 317356B1 NO 19982561 A NO19982561 A NO 19982561A NO 982561 A NO982561 A NO 982561A NO 317356 B1 NO317356 B1 NO 317356B1
- Authority
- NO
- Norway
- Prior art keywords
- hydroxy
- tax
- oxo
- epoxy
- butoxycarbonylamino
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title claims abstract description 4
- AMDOWEDYDFGDJI-IREPQIBFSA-N (2r,3s)-2-hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid;dihydrate Chemical compound O.O.CC(C)(C)OC(=O)N[C@H]([C@@H](O)C(O)=O)C1=CC=CC=C1 AMDOWEDYDFGDJI-IREPQIBFSA-N 0.000 title description 5
- ZVAFCKLQJCZGAP-WDEREUQCSA-N (2r,3s)-2-hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid Chemical compound CC(C)(C)OC(=O)N[C@H]([C@@H](O)C(O)=O)C1=CC=CC=C1 ZVAFCKLQJCZGAP-WDEREUQCSA-N 0.000 claims abstract description 18
- 150000004683 dihydrates Chemical class 0.000 claims abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 34
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 20
- 238000001035 drying Methods 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical group CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 8
- 150000002576 ketones Chemical class 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 238000010511 deprotection reaction Methods 0.000 claims description 2
- 238000003860 storage Methods 0.000 claims description 2
- -1 (2R,3S)-3-tert-butoxycarbonylamino-2-hydroxy-3-phenylpropionate carboxylate Chemical class 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 238000002425 crystallisation Methods 0.000 abstract 1
- 230000008025 crystallization Effects 0.000 abstract 1
- 238000010586 diagram Methods 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 239000000725 suspension Substances 0.000 description 8
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 238000001914 filtration Methods 0.000 description 4
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- ZVAFCKLQJCZGAP-UHFFFAOYSA-N 2-hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid Chemical compound CC(C)(C)OC(=O)NC(C(O)C(O)=O)C1=CC=CC=C1 ZVAFCKLQJCZGAP-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 230000000719 anti-leukaemic effect Effects 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D305/00—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms
- C07D305/14—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms condensed with carbocyclic rings or ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Epoxy Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9514841A FR2742438B1 (fr) | 1995-12-14 | 1995-12-14 | Dihydrate du (2r,3s)-3-tert-butoxycarbonylamino-2-hydroxy- 3-phenylpropionate de 4,10beta-diacetoxy-2alpha-benzoyloxy- 5beta,2o-epoxy-1-hydroxy-9-oxo-19-nor-cyclopropa(g)tax-11- ene-13alpha-yle, et son procede de preparation |
PCT/FR1996/001957 WO1997021695A1 (fr) | 1995-12-14 | 1996-12-09 | DIHYDRATE DU (2R,3S)-3-TERT-BUTOXYCARBONYLAMINO-2-HYDROXY-3-PHENYLPROPIONATE DE 4,10β-DIACETOXY-2α-BENZOYLOXY-5β,20-EPOXY-1-HYDROXY-9-OXO-19-NOR-CYCLOPROPA[G]TAX-11-ENE-13α-YLE, ET SON PROCEDE DE PREPARATION |
Publications (3)
Publication Number | Publication Date |
---|---|
NO982561D0 NO982561D0 (no) | 1998-06-04 |
NO982561L NO982561L (no) | 1998-06-04 |
NO317356B1 true NO317356B1 (no) | 2004-10-18 |
Family
ID=9485512
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO19982561A NO317356B1 (no) | 1995-12-14 | 1998-06-04 | 4,10beta-diacetoksy-2alfa-benzoyloksy-5beta,20-epoksy-1-hydroksy-9-okso-19-nor-cyklopropa[G]tax-11-en-13<alfa>-yl (2R,3S)-3-tert-butoksykarbonylamino-2-hydroksy-3-fenylpropionat dihydrat, samt fremstilling derav |
Country Status (37)
Country | Link |
---|---|
EP (1) | EP0876361B1 (de) |
JP (1) | JP4059351B2 (de) |
KR (1) | KR100429330B1 (de) |
CN (1) | CN101113143A (de) |
AR (1) | AR004380A1 (de) |
AT (1) | ATE204573T1 (de) |
AU (1) | AU713086C (de) |
BG (1) | BG63010B1 (de) |
BR (1) | BR9611957A (de) |
CA (1) | CA2236545C (de) |
CO (1) | CO4810227A1 (de) |
CZ (1) | CZ288998B6 (de) |
DE (1) | DE69614716T2 (de) |
DK (1) | DK0876361T3 (de) |
DZ (1) | DZ2140A1 (de) |
EA (1) | EA000668B1 (de) |
ES (1) | ES2162123T3 (de) |
FR (1) | FR2742438B1 (de) |
GR (1) | GR3036437T3 (de) |
HU (1) | HU224962B1 (de) |
IL (1) | IL124766A (de) |
IN (1) | IN185809B (de) |
MY (1) | MY115886A (de) |
NO (1) | NO317356B1 (de) |
NZ (1) | NZ323964A (de) |
OA (1) | OA11012A (de) |
PL (1) | PL187613B1 (de) |
PT (1) | PT876361E (de) |
RO (1) | RO115880B1 (de) |
SK (1) | SK282512B6 (de) |
TN (1) | TNSN96157A1 (de) |
TR (1) | TR199801087T2 (de) |
TW (1) | TW358093B (de) |
UA (1) | UA55401C2 (de) |
UY (1) | UY24387A1 (de) |
WO (1) | WO1997021695A1 (de) |
ZA (1) | ZA9610200B (de) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102851740A (zh) * | 2011-06-30 | 2013-01-02 | 复旦大学 | 一种氟代多烯紫杉醇晶体及其制备方法 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2698871B1 (fr) * | 1992-12-09 | 1995-02-24 | Rhone Poulenc Rorer Sa | Nouveau taxoïdes, leur préparation et les compositions pharmaceutiques qui les contiennent. |
-
1995
- 1995-12-14 FR FR9514841A patent/FR2742438B1/fr not_active Expired - Fee Related
-
1996
- 1996-09-12 UA UA98063068A patent/UA55401C2/uk unknown
- 1996-12-02 UY UY24387A patent/UY24387A1/es not_active IP Right Cessation
- 1996-12-04 TW TW085114946A patent/TW358093B/zh not_active IP Right Cessation
- 1996-12-04 ZA ZA9610200A patent/ZA9610200B/xx unknown
- 1996-12-09 DK DK96941720T patent/DK0876361T3/da active
- 1996-12-09 DE DE69614716T patent/DE69614716T2/de not_active Expired - Lifetime
- 1996-12-09 AU AU11013/97A patent/AU713086C/en not_active Ceased
- 1996-12-09 KR KR10-1998-0704420A patent/KR100429330B1/ko not_active IP Right Cessation
- 1996-12-09 CZ CZ19981830A patent/CZ288998B6/cs not_active IP Right Cessation
- 1996-12-09 DZ DZ960185A patent/DZ2140A1/fr active
- 1996-12-09 RO RO98-01069A patent/RO115880B1/ro unknown
- 1996-12-09 SK SK790-98A patent/SK282512B6/sk not_active IP Right Cessation
- 1996-12-09 WO PCT/FR1996/001957 patent/WO1997021695A1/fr active IP Right Grant
- 1996-12-09 HU HU9904048A patent/HU224962B1/hu not_active IP Right Cessation
- 1996-12-09 EA EA199800452A patent/EA000668B1/ru not_active IP Right Cessation
- 1996-12-09 CA CA002236545A patent/CA2236545C/fr not_active Expired - Fee Related
- 1996-12-09 PL PL96327451A patent/PL187613B1/pl not_active IP Right Cessation
- 1996-12-09 IL IL12476696A patent/IL124766A/xx not_active IP Right Cessation
- 1996-12-09 ES ES96941720T patent/ES2162123T3/es not_active Expired - Lifetime
- 1996-12-09 TR TR1998/01087T patent/TR199801087T2/xx unknown
- 1996-12-09 EP EP96941720A patent/EP0876361B1/de not_active Expired - Lifetime
- 1996-12-09 CN CNA2007101024535A patent/CN101113143A/zh active Pending
- 1996-12-09 NZ NZ323964A patent/NZ323964A/xx not_active IP Right Cessation
- 1996-12-09 AT AT96941720T patent/ATE204573T1/de active
- 1996-12-09 JP JP52179097A patent/JP4059351B2/ja not_active Expired - Fee Related
- 1996-12-09 PT PT96941720T patent/PT876361E/pt unknown
- 1996-12-09 BR BR9611957A patent/BR9611957A/pt not_active IP Right Cessation
- 1996-12-12 IN IN2788DE1996 patent/IN185809B/en unknown
- 1996-12-13 MY MYPI96005258A patent/MY115886A/en unknown
- 1996-12-13 TN TNTNSN96157A patent/TNSN96157A1/fr unknown
- 1996-12-13 AR ARP960105668A patent/AR004380A1/es active IP Right Grant
- 1996-12-13 CO CO96065734A patent/CO4810227A1/es unknown
-
1998
- 1998-06-04 NO NO19982561A patent/NO317356B1/no not_active IP Right Cessation
- 1998-06-12 BG BG102535A patent/BG63010B1/bg unknown
- 1998-06-15 OA OA9800085A patent/OA11012A/fr unknown
-
2001
- 2001-08-23 GR GR20010400773T patent/GR3036437T3/el not_active IP Right Cessation
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6022985A (en) | Process for the preparation of 4-acetoxy-2α-benzoyloxy-5β, 20-epoxy-1, 7β-10β-trihydroxy-9-oxo-tax-11-en-13α-yl(2R,3S)-3-tert-b utoxy-carbonYlamino-2-hydroxy-3-phenylpropionate trihydrate | |
EP0026044B1 (de) | Aminsalz der Clavulansäure, seine Herstellung und Verwendung | |
US5391770A (en) | Process for preparing ascorbic acid | |
CZ54495A3 (en) | Process for preparing and/or purification of clavulanic acid | |
US5057615A (en) | Process for purifying tryptophan | |
NO156168B (no) | Fremgangsmaate ved fremstilling av den terapeutisk aktive krystallinske, hydratiserte form, betegnet <<form d>>, av natriumsaltet av syn-isomer 3-acetoxymethyl-7-(2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido)-cef-3-em-4-carb | |
FI75571B (fi) | Framstaellningsfoerfarande foer synnerligen kristalliniskt natriumcefoperazon. | |
NO317356B1 (no) | 4,10beta-diacetoksy-2alfa-benzoyloksy-5beta,20-epoksy-1-hydroksy-9-okso-19-nor-cyklopropa[G]tax-11-en-13<alfa>-yl (2R,3S)-3-tert-butoksykarbonylamino-2-hydroksy-3-fenylpropionat dihydrat, samt fremstilling derav | |
US4904776A (en) | Method for producing crystalline cefadroxil hemihydrate | |
EP0976750A1 (de) | Neue z-valacyclovir-kristalle | |
CN108358979B (zh) | 泰万菌素的纯化方法 | |
US4219641A (en) | Process for preparing erythromycin succinate | |
NO167460B (no) | Fremgangsmaate til rensing av et antibiotikumholdig materiale. | |
GB2085884A (en) | Crystals of beta -nicotinamide- adenine-dinucleotide and process for preparing the same | |
NO327178B1 (no) | Fremgangsmate for fremstilling av 3,4-metylendioksy-mandelsyre | |
US5614651A (en) | 14α-hydroxy-4-androstene-3,6,17-trione hydrate crystal and process for producing same | |
US2421142A (en) | Process for obtaining crystalline riboflavin | |
EP0293244A2 (de) | N-epsilon-trifluoroacetyl-L-lysyl-L-prolin,D-10-camphorsulphonsäuresalz und Verfahren zu dessen Herstellung | |
MXPA98004604A (en) | Dihydrate (2r, 3s) -3-ter-butoxicarbonilamino-2-hidroxi-3-fenilpropionato de 4, iobeta-diacetoxi-2alfa-benzoiloxi-5beta, 20-epoxi-1-hidroxi-9-oxo-19-nor- ciclopropa [g] tax-11- en-13alfa-ilo, and its preparation procedure | |
HU206724B (en) | Process for producing intermediate of beta-lactamase inhibitor | |
JP3815064B2 (ja) | 1−(4−クロロベンゾイル)−5−メトキシ−2−メチルインドール−3−酢酸の精製方法 | |
GB2033382A (en) | Production of N-(4'-Chloro-3- sulphamoyl-benzenesulphonyl)-N- methyl-2-aminomethyl-2-methyl tetrahydrofuran | |
JP3810842B2 (ja) | イソオキサゾール誘導体のCa塩2水和物の製造法 | |
RU2083565C1 (ru) | Способ получения 1-фенил-3-метилпиразолона-5 | |
CN111217781A (zh) | 贝前列素-314d晶体和其制备方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM1K | Lapsed by not paying the annual fees |