Process for the preparation of 17-substituted-delta4-gonenes and intermediates
    2.
    发明授权
    Process for the preparation of 17-substituted-delta4-gonenes and intermediates 失效
    制备17-取代的DELTA4-GONENES和中间体的方法

    公开(公告)号:US3843686A

    公开(公告)日:1974-10-22

    申请号:US26736472

    申请日:1972-06-29

    Applicant: ROUSSEL UCLAF

    CPC classification number: C07J73/00 C07J1/00 C07J7/00 C07J41/00 C07J75/00

    Abstract: WHEREIN R represents a member selected from the group consisting of hydrogen and the acyl of an organic carboxylic acid having from one to 18 carbon atoms, R'' represents an alkyl having from one to four carbon atoms, Riv represents a member selected from the group consisting of lower alkyl, lower alkenyl or lower alkynyl, and B represents a member selected from the group consisting of two hydrogens in the 9 Alpha and 10 Beta position and a double bond which comprises the steps of reacting a 3ketal-4,5-seco-gonane-5-one with a ketalizing agent, oxidizing the resultant 3,5-diketal-4,5-seco-gonane-17 Beta -ol, reacting the resultant 3,5-diketal-4,5-seco-gonane-17-one with an organometallic compound, hydrolyzing the resultant 3,5-diketal17 Alpha -Riv-4,5-seco-gonane-17 Beta -ol, cyclizing the resultant 17 Alpha -Riv-4,5-seco-gonane-17 Beta -ol-3,5-dione and recovering said Delta 4-gonenic steroid. The novel intermediates are also part of the invention. The Delta 4-gonenic steroids are known compounds having steroidal properties.

    A process for the production of a Delta 4-gonenic steroid having the formula

    Novel 19-nor delta 4,9-pregnadienes
    3.
    发明授权
    Novel 19-nor delta 4,9-pregnadienes 失效
    新一代19-NOR DELTA 4,9-PREGNADIENES

    公开(公告)号:US3721685A

    公开(公告)日:1973-03-20

    申请号:US3721685D

    申请日:1971-03-01

    Applicant: ROUSSEL UCLAF

    Inventor: JOLLY J PIERDET A

    CPC classification number: C07D295/215 Y10S514/842 Y10S514/843

    Abstract: 13B-R-17A-METHYL-18,19-DINOR$4,9-PREGNADIENES OF THE FORMULA

    17-(H3C-),17-(R''-O-CH(-CH3)-),18-R-4,9-GONADIEN-3-ONE

    WHEREIN R IS ALKYL OF 1 TO 4 CARBON ATOMS AND R'' IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN AND ACYL OF AN ORGANIC CARBOXYLIC ACID OF 1 TO 18 CARBON ATOMS HAVING ANTI-OVULATORY ACTIVITY AND THEIR PREPARATON AND INTERMEDIATES THEREOF.

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