ATE747T1 - 7A-METHYL-ESTROGENS AND PROCESSES FOR THEIR PRODUCTION AND THEIR USE FOR FURTHER PROCESSING. - Google Patents

7A-METHYL-ESTROGENS AND PROCESSES FOR THEIR PRODUCTION AND THEIR USE FOR FURTHER PROCESSING.

Info

Publication number
ATE747T1
ATE747T1 AT79102370T AT79102370T ATE747T1 AT E747 T1 ATE747 T1 AT E747T1 AT 79102370 T AT79102370 T AT 79102370T AT 79102370 T AT79102370 T AT 79102370T AT E747 T1 ATE747 T1 AT E747T1
Authority
AT
Austria
Prior art keywords
general formula
compound
group
see diagramm
meanings given
Prior art date
Application number
AT79102370T
Other languages
German (de)
Inventor
Gerhard Dr. Sauer
Ulrich Dr. Eder
Gregor Dr. Haffer
Guenter Dr. Neef
Rudolf Prof. Dr. Wiechert
Original Assignee
Schering Aktiengesellschaft Berlin Und Bergkamen
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 Schering Aktiengesellschaft Berlin Und Bergkamen filed Critical Schering Aktiengesellschaft Berlin Und Bergkamen
Application granted granted Critical
Publication of ATE747T1 publication Critical patent/ATE747T1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C317/00—Sulfones; Sulfoxides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07J—STEROIDS
    • C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
    • C07J1/0051—Estrane derivatives
    • C07J1/0066—Estrane derivatives substituted in position 17 beta not substituted in position 17 alfa
    • C07J1/007—Estrane derivatives substituted in position 17 beta not substituted in position 17 alfa the substituent being an OH group free esterified or etherified
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07J—STEROIDS
    • C07J31/00—Normal steroids containing one or more sulfur atoms not belonging to a hetero ring
    • C07J31/006—Normal steroids containing one or more sulfur atoms not belonging to a hetero ring not covered by C07J31/003
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07J—STEROIDS
    • C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
    • C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
    • C07J41/0094—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 containing nitrile radicals, including thiocyanide radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Steroid Compounds (AREA)
  • Cosmetics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

For the Contracting States : BE, CH, DE, FR, GB, IT, LU, NL, SE. 1. 7alpha-methyl oestrogens of the general formula I see diagramm : EP0007515,P12,F1 in which R1 and R2 represent a lower alkyl group having from 1 to 4 carbon atoms, Z represents a hydrogen atom or an OR1 group, and X represents a functionally protected hydroxymethylene group. 1.For the Contracting State : AT. 1. Process for the manufacture of 7alpha-methyl oestrogens of the general formula I see diagramm : EP0007515,P17,F1 in which R1 and R2 represent a lower alkyl group having from 1 to 4 carbon atoms, Z represents a hydrogen atom or an OR1 group, and X represents a functionally protected hydroxymethylene group, characterized in that, in a manner known per se, a) a compound of the general formula II see diagramm : EP0007515,P17,F2 in which R1 and Z have the meanings given in claim 1 and Y represents a -C-=N group or an optionally esterified -COOH or -SO2 R3 group, R3 representing a lower or middle alkyl group having from 1 to 8 carbon atoms or an optionally substituted aryl group, is reacted, in the presence of a deprotonating agent, with a compound of the general formula III see diagramm : EP0007515,P17,F3 in which X and R2 have the meanings given in claim 1 and R3 has the meaning given above, yielding a compound of the general formula IV see diagramm : EP0007515,P18,F4 in which R1 , R2 , X, Z and Y have the meanings given above ; b) the compound of the general formula IV is cyclised to form a compound of the general formula V see diagramm : EP0007515,P18,F5 in which R1 , R2 , X, Y and Z have the meanings given above ; c) the compound of the general formula V is hydrogenated in the presence of a noble metal catalyst to form a compound of the general formula VI see diagramm : EP0007515,P18,F6 in which R1 , R2 , X, Y and Z have the meanings given above ; d) the compound of the general formula VI is oxidised to form a compound of the general formula VII see diagramm : EP0007515,P18,F7 in which R1 , R2 , Z and X have the meanings given above ; e) the compounds of the general formula VII are methylated.
AT79102370T 1978-07-21 1979-07-11 7A-METHYL-ESTROGENS AND PROCESSES FOR THEIR PRODUCTION AND THEIR USE FOR FURTHER PROCESSING. ATE747T1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19782832606 DE2832606A1 (en) 1978-07-21 1978-07-21 METHOD FOR PRODUCING 7 ALPHA METHYL OESTROGENES
EP79102370A EP0007515B1 (en) 1978-07-21 1979-07-11 7a-methyl estrogens and process for their preparation and their use in further processing

Publications (1)

Publication Number Publication Date
ATE747T1 true ATE747T1 (en) 1982-03-15

Family

ID=6045336

Family Applications (1)

Application Number Title Priority Date Filing Date
AT79102370T ATE747T1 (en) 1978-07-21 1979-07-11 7A-METHYL-ESTROGENS AND PROCESSES FOR THEIR PRODUCTION AND THEIR USE FOR FURTHER PROCESSING.

Country Status (3)

Country Link
EP (1) EP0007515B1 (en)
AT (1) ATE747T1 (en)
DE (2) DE2832606A1 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001058919A2 (en) * 2000-02-11 2001-08-16 Sri International Synthesis of anti-estrogenic and other therapeutic steroids from 21-hydroxy-19-norpregna-4-en-3-one
US10174070B2 (en) 2005-09-30 2019-01-08 Endece Llc 6-substituted estradiol derivatives and methods of use
CN115353540B (en) * 2022-09-21 2023-08-11 中国科学院上海有机化学研究所 A kind of synthetic method and application of phenolic steroid compound

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE793252A (en) * 1971-12-24 1973-06-22 Schering Ag NEW DICYCLOALKANE DERIVATIVES AND THEIR PREPARATION PROCESS
DE2253089C2 (en) * 1972-10-25 1983-01-13 Schering Ag, 1000 Berlin Und 4619 Bergkamen 9-Oxo-9,10, seco-oestran derivatives and processes for the preparation of these compounds and of 9-oxo-D-homo-9,10-seco-oestran derivatives
US4064173A (en) * 1973-12-21 1977-12-20 Hoffmann-La Roche, Inc. 9,10-Seco-steroids

Also Published As

Publication number Publication date
DE2962254D1 (en) 1982-04-08
EP0007515B1 (en) 1982-03-10
EP0007515A1 (en) 1980-02-06
DE2832606A1 (en) 1980-01-31

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Legal Events

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REN Ceased due to non-payment of the annual fee