BG44029A3 - Method for preparing of n- dimethyl morphinanic derivatives - Google Patents

Method for preparing of n- dimethyl morphinanic derivatives

Info

Publication number
BG44029A3
BG44029A3 BG8571084A BG7108485A BG44029A3 BG 44029 A3 BG44029 A3 BG 44029A3 BG 8571084 A BG8571084 A BG 8571084A BG 7108485 A BG7108485 A BG 7108485A BG 44029 A3 BG44029 A3 BG 44029A3
Authority
BG
Bulgaria
Prior art keywords
group
hydrogen atom
carbon atoms
benzoyloxy
acyloxy
Prior art date
Application number
BG8571084A
Inventor
Sandor Hosztafi
Tibor Timar
Julianna Nagy
Ilona Fabian
Original Assignee
Alkaloida Vegyeszety Gyar,Hu
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 Alkaloida Vegyeszety Gyar,Hu filed Critical Alkaloida Vegyeszety Gyar,Hu
Publication of BG44029A3 publication Critical patent/BG44029A3/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D489/00Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula:
    • C07D489/02Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula: with oxygen atoms attached in positions 3 and 6, e.g. morphine, morphinone
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D489/00Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula:
    • C07D489/06Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula: with a hetero atom directly attached in position 14
    • C07D489/08Oxygen atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Ultra Sonic Daignosis Equipment (AREA)
  • Stringed Musical Instruments (AREA)
  • Electrophonic Musical Instruments (AREA)
  • Cephalosporin Compounds (AREA)
  • Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Finger-Pressure Massage (AREA)
  • Measurement And Recording Of Electrical Phenomena And Electrical Characteristics Of The Living Body (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Materials For Photolithography (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)

Abstract

1. Process for the preparation of compounds having the N-demethylmorphinane structure of the general formula (III) see diagramm : EP0168686,P8,F1 wherein Z is CH2 -CH2 or CH=CH, Y is an oxygen atom or a group R3 and R4 wherein R3 is a hydrogen atom, a hydroxy group, an acyloxy group having from 1 to 3 carbon atoms or a benzoyloxy group, its spatial configuration being alpha, R4 is a hydrogen atom, a halogen atom, a hydroxy group, an alkyl group having from 1 to 3 carbon atoms, an acyloxy group having from 1 to 3 carbon atoms, a benzoyloxy or azido group, its spatial configuration being beta, R2 is hydrogen atom, an acyloxy group having from 1 to 3 carbon atoms or a benzoyloxy group, R1 is a hydrogen atom, an alkyl group having from 1 to 5 carbon atoms, an aryl or aralkyl group, an acyl group having from 1 to 3 carbon atoms or a benzoyl group, with the proviso that when R3 is a hydrogen atom, a hydroxy group, an acyloxy or benzoyloxy group, R4 is a hydrogen atom or an alkyl group, and when R4 is a hydrogen atom, a halogen atom, a hydroxy group, an acyloxy, benzoyloxy or azido group, R3 is a hydrogen atom, by reaction of morphinane alkaloids of the general formula (I) see diagramm : EP0168686,P9,F2 in which Z, Y, R1 and R2 have the definitions given above, with phosgene or diphosgene at a temperature of from 0 to 1208C in a solvent, and subsequent hydrolysis of the resulting N-chlorocarbonyl-N-demethyl derivative of the general formula (II) see diagramm : EP0168686,P9,F3 in which Z, Y, R1 and R2 have the meanings given above, with a mineral acid, which process is characterized in that the reaction with phosgene or diphosgene is carried out in 1,2-dichloroethane in the presence of alkali metal carbonates or alkali metal hydrogen carbonates, and then, without isolation, the resulting N-chlorocarbonyl-N-demethyl derivative of the general formula (II) is heated with 5 % hydrochloric acid.
BG8571084A 1984-07-17 1985-07-15 Method for preparing of n- dimethyl morphinanic derivatives BG44029A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
HU842774A HU197750B (en) 1984-07-17 1984-07-17 Process for n-demethylation of morphine alkaloids

Publications (1)

Publication Number Publication Date
BG44029A3 true BG44029A3 (en) 1988-09-15

Family

ID=10961043

Family Applications (1)

Application Number Title Priority Date Filing Date
BG8571084A BG44029A3 (en) 1984-07-17 1985-07-15 Method for preparing of n- dimethyl morphinanic derivatives

Country Status (18)

Country Link
EP (1) EP0168686B1 (en)
JP (1) JPS6193184A (en)
AT (1) ATE41933T1 (en)
BG (1) BG44029A3 (en)
CS (1) CS251792B2 (en)
DD (1) DD235639A5 (en)
DE (1) DE3569244D1 (en)
DK (1) DK322385A (en)
ES (1) ES8603716A1 (en)
FI (1) FI81583C (en)
HU (1) HU197750B (en)
IL (2) IL75509A0 (en)
IN (1) IN166255B (en)
NO (1) NO161915C (en)
PL (1) PL254552A1 (en)
RO (1) RO91516B (en)
SU (1) SU1398776A3 (en)
YU (1) YU45264B (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2008338970B2 (en) * 2007-12-17 2013-08-22 SpecGx LLC Sinomenine derivatives and processes for their synthesis
US8252808B2 (en) 2007-12-17 2012-08-28 Mallinckrodt Llc Process and compounds for the production of (+)opiates
US8362283B2 (en) * 2009-05-12 2013-01-29 Board Of Regents, The University Of Texas System Cross-conjugated 2,5-cyclohexadienone and related synthesis methods
JP5911484B2 (en) * 2010-07-16 2016-04-27 マリンクロッド エルエルシー (+)-Morphinan as an antagonist of Toll-like receptor 9 and its therapeutic use
KR20140063763A (en) 2011-09-08 2014-05-27 말린크로트 엘엘씨 Production of alkaloids without the isolation of intermediates

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE367407B (en) * 1967-08-04 1974-05-27 Boehringer Sohn Ingelheim
DE2254298A1 (en) * 1972-11-06 1974-05-16 Boehringer Sohn Ingelheim Heteroarylmethyl-normorphines prepn - by alkylation of normorphine etc., antidotes for opiate poisoning
DE2727805A1 (en) * 1977-06-21 1979-01-04 Goedecke Ag METHOD FOR PRODUCING OXYNORMORPHONE

Also Published As

Publication number Publication date
CS251792B2 (en) 1987-08-13
FI852779L (en) 1986-01-18
IL78503A (en) 1990-01-18
HUT38645A (en) 1986-06-30
EP0168686B1 (en) 1989-04-05
DE3569244D1 (en) 1989-05-11
DK322385D0 (en) 1985-07-15
FI852779A0 (en) 1985-07-15
DD235639A5 (en) 1986-05-14
ATE41933T1 (en) 1989-04-15
ES8603716A1 (en) 1986-01-16
JPS6193184A (en) 1986-05-12
IN166255B (en) 1990-03-31
NO852838L (en) 1986-01-20
YU117485A (en) 1988-04-30
DK322385A (en) 1986-01-18
FI81583B (en) 1990-07-31
FI81583C (en) 1990-11-12
YU45264B (en) 1992-05-28
PL254552A1 (en) 1986-07-15
NO161915C (en) 1989-10-11
NO161915B (en) 1989-07-03
RO91516B (en) 1987-07-01
HU197750B (en) 1989-05-29
IL75509A0 (en) 1985-10-31
CS528085A2 (en) 1986-12-18
ES544385A0 (en) 1986-01-16
EP0168686A1 (en) 1986-01-22
RO91516A (en) 1987-06-30
SU1398776A3 (en) 1988-06-15

Similar Documents

Publication Publication Date Title
BG44029A3 (en) Method for preparing of n- dimethyl morphinanic derivatives
CS909186A2 (en) Zpusob vyroby chinolinkarboxylovych kyselin
HUT53628A (en) Process for selective etherification
JPS5559127A (en) Novel intermediate compound for producing prostanoids and its manufacture
HUT40995A (en) Process for producing esters of 4-/acyloxy/-3-oxo-butiric acid
FR2528828B1 (en)
DE3465737D1 (en) Process for the preparation of 4-quinolinones
PL296513A1 (en) Method of obtaining 20-oxo-17 alpha,21-dihydroxyl derivatives of pregnane and novel intermediate products
KR860009006A (en) Method for preparing 2-thiochromenilideneacetoacetic acid ester
DE3462035D1 (en) Process for the preparation of 4-quinolinones
DE3368632D1 (en) Process for the preparation of lysergic acid esters