GB1368005A - 17-hydroxy-7-/lower alkoxy/carbonyl-3-oxo-17alpha-pregn-4-ene-21- carboxylic acid ypsilon-lactones and congeners - Google Patents

17-hydroxy-7-/lower alkoxy/carbonyl-3-oxo-17alpha-pregn-4-ene-21- carboxylic acid ypsilon-lactones and congeners

Info

Publication number
GB1368005A
GB1368005A GB3940172A GB3940172A GB1368005A GB 1368005 A GB1368005 A GB 1368005A GB 3940172 A GB3940172 A GB 3940172A GB 3940172 A GB3940172 A GB 3940172A GB 1368005 A GB1368005 A GB 1368005A
Authority
GB
United Kingdom
Prior art keywords
compound
alkyl
give
carboxylic acid
contacting
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
GB3940172A
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.)
GD Searle LLC
Original Assignee
GD Searle LLC
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 GD Searle LLC filed Critical GD Searle LLC
Publication of GB1368005A publication Critical patent/GB1368005A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J9/00Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane
    • C07J9/005Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane containing a carboxylic function directly attached or attached by a chain containing only carbon atoms to the cyclopenta[a]hydrophenanthrene skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J21/00Normal steroids containing carbon, hydrogen, halogen or oxygen having an oxygen-containing hetero ring spiro-condensed with the cyclopenta(a)hydrophenanthrene skeleton
    • C07J21/001Lactones
    • C07J21/003Lactones at position 17

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Steroid Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1368005 7-Carboxy steroids and related compounds G D SEARLE & CO 24 Aug 1972 [25 Aug 1971] 39401/72 Heading C2U Novel steroids have the formulµ wherein Z is H, alkali metal, alkaline earth metal/2, ammonium or alkyl; Z<SP>1</SP> is H, alkali metal, alkaline earth metal/2 or ammonium when Z is alkyl and is identical to Z when Z is H, alkali metal, alkaline-earth metal/2 or ammonium; the #<SP>1</SP> double bond is optional; the wavy line indicates the alternative α and # configurations; and X is oxygen, and it may also be sulphur when Z is alkyl and #<SP>1</SP> is absent in (Ia). They are prepared by (a) contacting 4α,7α - carbonyl - 5 - cyano - 17 - hydroxy - 3- oxo - 5#,17α - pregnane - 21 - carboxylic acid γ-lactone with an alkali metal alkoxide to afford a mixture of 7α and 7# compounds (Ia) wherein X is O, Z is alkyl and #<SP>1</SP> is absent, which may be separated by conventional procedures; (b) contacting an active acylating derivative of a compound (Ia) wherein X is O and Z is H, particularly a novel compound of the formula with an alkanol to give compounds (Ia) wherein X is O and Z is alkyl, the acylating derivatives (II) being prepared from the corresponding 7- carboxylic acids (Ia) and alkyl chloroformates in the presence of a tertiary amine; (c) dehydrogenating a compound (Ia) wherein X is O, Z is alkyl and #<SP>1</SP> is absent to give the corresponding #<SP>1,4</SP> compound, using, for example, 2,3-dichloro - 5,6 - dicyano - 1,4 - benzoquinone; (d) reacting a compound (Ia) wherein X is O and Z is alkyl or H with, respectively, one or two equivalents of a base, e.g. KOH, in an aqueous medium, to give the corresponding mono- or bis-metal salt (Ib) followed, when required, by brief exposure to a proton source to give the corresponding mono- or di-carboxylic acid (Ib); (e) hydrolysing under alkaline conditions a compound (Ia) wherein X is O and Z is alkyl followed by mineral acid treatment to give a compound (Ia) wherein X is O and Z is H; (f) contacting a starting material as defined in (b) above with an alkane thiol to give a compound (Ia) wherein X is S, Z is alkyl and #<SP>1</SP> is absent; (g) contacting a starting material as defined in (a) above with KOH in methanol followed by alkaline hydrolysis and subsequent mineral acid treatment to give a corresponding 7α compound (Ia) wherein X is O, Z is H and #<SP>1</SP> is absent; (h) contacting a compound (Ia) or (Ib) wherein X is O, Z is H or alkyl and Z<SP>1</SP> is H which contains at least one acid hydrogen with an appropriate quantity of a base in an aqueous medium to give a corresponding mono- or bis-metal salt of a compound (Ia) or (Ib); or (i) contacting a compound (Ia) wherein X is O and Z is H or a compound (Ib) wherein X is O, Z is H or alkyl and Z<SP>1</SP> is H with excess ammonia to give a corresponding ammonium salt. 4α,7α - Carbonyl - 5 - cyano - 17 - hydroxy - 3- oxo - 5#,17α - pregnane - 21 - carboxylic acid γ-lactone is prepared by heating 17-hydroxy-3- oxo - 17α - pregna - 4,6 - diene - 21 - carboxylic acid γ-lactone with an alkali metal cyanide under slightly basic conditions in a solvent followed by heating the resulting 7α,4-aminomethylidyne - 5 - cyano - 17 - hydroxy - 3 - oxo- 5#,17α - pregnane - 21 - carboxylic acid γ- lactone with very dilute aqueous mineral acid (see Specification 1,368,006). The novel steroids of the Formulµ (Ia) and (Ib) are diuretic and blood pressure-lowering agents. They may be made up into pharmaceutical compositions with suitable carriers.
GB3940172A 1971-08-25 1972-08-24 17-hydroxy-7-/lower alkoxy/carbonyl-3-oxo-17alpha-pregn-4-ene-21- carboxylic acid ypsilon-lactones and congeners Expired GB1368005A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US17492271A 1971-08-25 1971-08-25

Publications (1)

Publication Number Publication Date
GB1368005A true GB1368005A (en) 1974-09-25

Family

ID=22638078

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3940172A Expired GB1368005A (en) 1971-08-25 1972-08-24 17-hydroxy-7-/lower alkoxy/carbonyl-3-oxo-17alpha-pregn-4-ene-21- carboxylic acid ypsilon-lactones and congeners

Country Status (21)

Country Link
JP (2) JPS5839840B2 (en)
AT (1) AT323907B (en)
AU (1) AU475957B2 (en)
BE (1) BE787940A (en)
CA (1) CA970361A (en)
CH (2) CH601350A5 (en)
DE (1) DE2241680C2 (en)
DK (1) DK133954B (en)
ES (2) ES406044A1 (en)
FI (1) FI50429C (en)
FR (1) FR2150852B1 (en)
GB (1) GB1368005A (en)
IE (1) IE36653B1 (en)
IL (1) IL40197A (en)
KE (1) KE2813A (en)
MY (1) MY7800121A (en)
NL (1) NL176569C (en)
NO (1) NO134990C (en)
PH (1) PH9271A (en)
SE (2) SE380533B (en)
ZA (1) ZA725839B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4069219A (en) * 1976-12-27 1978-01-17 G. D. Searle & Co. 7ξ-(Alkoxycarbonyl)-6ξ-alkyl/halo-17-hydroxy-3-oxo-17α-pregn-4-ene-21-carboxylic acid γ-lactones and corresponding 21-carboxylic acids, their salts, and esters
FR2496669A1 (en) * 1980-12-23 1982-06-25 Roussel Uclaf NOVEL STEROID 3-KETO4 OR 1-4 SUBSTITUTED DERIVATIVES IN POSITION 7, PROCESS FOR PREPARING THEM AND THEIR APPLICATION AS MEDICAMENTS
DE3111951A1 (en) * 1981-03-23 1982-09-30 Schering Ag, 1000 Berlin Und 4619 Bergkamen 7 (ALPHA) -ALKOXYCARBONYL-15SS-METHYLENE-4-ANDROSTENE, METHOD FOR THE PRODUCTION AND USE THEREOF AS A MEDICINAL PRODUCT
JPS57169230A (en) * 1981-04-10 1982-10-18 Matsushita Electric Ind Co Ltd Oil-immersed plastic ilm capacitor
US5296318A (en) * 1993-03-05 1994-03-22 Bell Communications Research, Inc. Rechargeable lithium intercalation battery with hybrid polymeric electrolyte
BRPI0515106A (en) * 2004-09-09 2008-07-08 Pharmacia Corp process for preparing substituted 7 (alpha) -alkoxycarbonyl steroids

Also Published As

Publication number Publication date
IE36653B1 (en) 1977-01-19
PH9271A (en) 1975-07-30
KE2813A (en) 1978-02-10
DK133954C (en) 1977-01-24
AU4578772A (en) 1974-02-28
ZA725839B (en) 1973-10-31
AU475957B2 (en) 1976-09-09
AT323907B (en) 1975-08-11
NL7211559A (en) 1973-02-27
NO134990C (en) 1977-01-26
FI50429C (en) 1976-03-10
JPS611080B2 (en) 1986-01-13
NL176569C (en) 1985-05-01
JPS5839840B2 (en) 1983-09-01
CH603689A5 (en) 1978-08-31
JPS4832860A (en) 1973-05-02
DK133954B (en) 1976-08-16
NO134990B (en) 1976-10-11
IL40197A0 (en) 1972-10-29
CA970361A (en) 1975-07-01
SE7415187L (en) 1974-12-04
CH601350A5 (en) 1978-07-14
IE36653L (en) 1973-02-25
IL40197A (en) 1976-05-31
FR2150852B1 (en) 1975-10-17
ES435189A1 (en) 1976-12-01
BE787940A (en) 1973-02-26
DE2241680C2 (en) 1982-09-09
MY7800121A (en) 1978-12-31
NL176569B (en) 1984-12-03
JPS5890598A (en) 1983-05-30
DE2241680A1 (en) 1973-03-01
SE380533B (en) 1975-11-10
ES406044A1 (en) 1976-01-16
FI50429B (en) 1975-12-01
SE404024B (en) 1978-09-18
FR2150852A1 (en) 1973-04-13

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee