CA1212108A - Methode de preparation d'un derive de l'oripavine - Google Patents

Methode de preparation d'un derive de l'oripavine

Info

Publication number
CA1212108A
CA1212108A CA000442036A CA442036A CA1212108A CA 1212108 A CA1212108 A CA 1212108A CA 000442036 A CA000442036 A CA 000442036A CA 442036 A CA442036 A CA 442036A CA 1212108 A CA1212108 A CA 1212108A
Authority
CA
Canada
Prior art keywords
endoethano
methyl
hydroxy
give
butyl
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
CA000442036A
Other languages
English (en)
Inventor
Navin Saxena
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Unichem Laboratories Ltd
Original Assignee
Unichem Laboratories Ltd
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.)
Filing date
Publication date
Application filed by Unichem Laboratories Ltd filed Critical Unichem Laboratories Ltd
Application granted granted Critical
Publication of CA1212108A publication Critical patent/CA1212108A/fr
Expired legal-status Critical Current

Links

Landscapes

  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
CA000442036A 1983-08-22 1983-11-28 Methode de preparation d'un derive de l'oripavine Expired CA1212108A (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IN259/BOM/83 1983-08-22
IN259/BOM/83A IN156632B (fr) 1983-08-22 1983-08-22

Publications (1)

Publication Number Publication Date
CA1212108A true CA1212108A (fr) 1986-09-30

Family

ID=11078963

Family Applications (1)

Application Number Title Priority Date Filing Date
CA000442036A Expired CA1212108A (fr) 1983-08-22 1983-11-28 Methode de preparation d'un derive de l'oripavine

Country Status (4)

Country Link
CA (1) CA1212108A (fr)
HU (1) HU193563B (fr)
IN (1) IN156632B (fr)
SU (1) SU1362734A1 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8357802B2 (en) 2006-10-17 2013-01-22 Penick Corporation Process for preparing oxymorphone
US9108974B2 (en) 2006-10-17 2015-08-18 Penick Corporation Process for preparing oxymorphone, naltrexone, and buprenorphine
EP2344507B1 (fr) 2008-09-30 2015-11-11 Mallinckrodt LLC Procédés d`augmentation du rendement de l'hydrolyse du groupe 3-o-méthyle et 17-n-nitrile dans la préparation de dérivés alcaloïdes opiacés

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2503677C1 (ru) * 2012-08-21 2014-01-10 Федеральное государственное бюджетное учреждение науки Институт элементоорганических соединений им. А.Н. Несмеянова Российской академии наук (ИНЭОС РАН) 3,6-диметокси-17-метил-7альфа-(трифторацетил)-4,5альфа-эпокси-6альфа,14альфа-этеноизоморфинан и способ его получения

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8357802B2 (en) 2006-10-17 2013-01-22 Penick Corporation Process for preparing oxymorphone
US9108974B2 (en) 2006-10-17 2015-08-18 Penick Corporation Process for preparing oxymorphone, naltrexone, and buprenorphine
US9487532B2 (en) 2006-10-17 2016-11-08 Penick Corporation Process for preparing oxymorphone, naltrexone, and buprenorphine
EP2344507B1 (fr) 2008-09-30 2015-11-11 Mallinckrodt LLC Procédés d`augmentation du rendement de l'hydrolyse du groupe 3-o-méthyle et 17-n-nitrile dans la préparation de dérivés alcaloïdes opiacés
EP2344507B2 (fr) 2008-09-30 2021-05-26 Mallinckrodt LLC Procédés d`augmentation du rendement de l'hydrolyse du groupe 3-o-méthyle et 17-n-nitrile dans la préparation de dérivés alcaloïdes opiacés

Also Published As

Publication number Publication date
IN156632B (fr) 1985-09-21
SU1362734A1 (ru) 1987-12-30
HUT39452A (en) 1986-09-29
HU193563B (en) 1987-10-28

Similar Documents

Publication Publication Date Title
CA1135691A (fr) 7 ET 7-8 SUBST. 4,5.alpha.-EPOXY-MORPHINAN-6- ONES
US4778891A (en) Certain pyrano (3,4-f)-indolizine derivatives
CA3026884C (fr) Procede de preparation de buprenorphine
OA10713A (en) Benzopyran and related ltb4 antagonists
JPS5827276B2 (ja) ビンカミンおよびその関連化合物の製法
CA1212108A (fr) Methode de preparation d'un derive de l'oripavine
US4272540A (en) 14-Methoxymorphinan-6-one compounds and therapeutic methods of treating pain and drug dependence with them
Schwartz et al. Biogenetically patterned synthesis of (+-)-cherylline
Hosztafi et al. Synthesis of N-Demethyl-N-Substituted-14-Hydroxycodeine and Morphine Derivatives+
Leland et al. Analgesic narcotic antagonists. 4. 7-Methyl-N-(cycloalkylmethyl)-3-hydroxy morphinan-6-one and-isomorphinan-6-one
JP3041022B2 (ja) 抗性物質m143―37f11の製造方法及び製造中間体
US3644373A (en) Method for the production of 3-substituted-1 2 3 4 5 6-hexahydro-6 11-dimethyl-8-hydroxy-2 6-methano-3-benzazocines
Csutoráas et al. A New and Efficient One-Pot Synthesis of Apomorphine and Its Ring-A Halogenated Derivatives1
Pearson et al. Alkylation of silyl ketene acetals with dienyliron complexes: application in the formation of quaternary carbon centers.
PL118827B1 (en) Method of manufacture of tricyclicdiketone
JPS6148839B2 (fr)
Riechers et al. Cyclization of 3‐Aminoacrylates–Total Synthesis of Pumiliotoxin C and Related Stereoisomeric Compounds
CA1135692A (fr) Composes 7-methyl et 7-methyl-8-alkyl inferieur b/c cis ou trans morphinan-6-ones
US4242514A (en) Method for the introduction of a methyl group into the 7 position of the morphinan nucleus
Lawson et al. Synthesis of morphine‐d5 and codeine‐d8
Tecle et al. Alkyl substituted 3‐PPP derivatives. Synthesis and biological investigation
JP3142273B2 (ja) 抗生物質mi43−37f11の製造中間体
HU188065B (en) New process for the dealkylation of tertiary amines
Huffman et al. Synthetie approaches to steroidal alkaloids III. An attempted synthesis of ring‐e of veratramine
Fraga et al. An unusual C-7 ortho ester from 6-epi-gibberellin A 13. X-Ray molecular structure of gibberellene C-7 ortho ester

Legal Events

Date Code Title Description
MKEX Expiry