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    Spiro benzocyclane acetic acid compounds
    31.
    发明授权
    Spiro benzocyclane acetic acid compounds 失效
    SPIRO BENZOCYCLANE乙酸化合物

    公开(公告)号：US3682964A

    公开(公告)日：1972-08-08

    申请号：US3682964D

    申请日：1970-08-31

    Applicant: ROUSSEL UCLAF

    Inventor： ROUSSEAU GENEVIEVE ,  ALLAIS ANDRES ,  POITTEVIN ANDRE

    IPC: C07C49/675 ,  C07C49/697 ,  C07C57/46 ,  C07C57/50 ,  C07C57/62 ,  C07C59/54 ,  C07C59/86 ,  C07C59/88 ,  C07D311/96 ,  A61K27/00 ,  C07D7/04 ,  C07D65/04

    CPC classification number: C07D311/96 ,  C07C49/675 ,  C07C49/697 ,  C07C57/46 ,  C07C57/50 ,  C07C57/62 ,  C07C59/54 ,  C07C59/86 ,  C07C59/88

    Abstract: Novel spiro benzocyclane acetic acid compounds of the formula

    WHEREIN R is selected from the group consisting of hydrogen and linear and branched alkyl of one to four carbon atoms, R1 is selected from the group consisting of hydrogen, chlorine, trifluoromethyl and lower alkoxy, Y is selected from the group consisting of methylene, oxygen and sulfur, n is 2, 3 or 4 and R2 is selected from the group consisting of hydrogen, substituted or unsubstituted alkyl of one to six carbon atoms and cation of nontoxic, pharmaceutically acceptable mineral and organic bases, processes for their preparation and novel intermediates. The compounds of formula I have analgesic and anti-inflammatory properties.

    Abstract translation: 式WHEREIN R的新型螺环苯并环丙烷乙酸化合物选自氢和1-4个碳原子的直链和支链烷基，R 1选自氢，氯，三氟甲基和低级烷氧基，Y是 选自亚甲基，氧和硫，n为2,3或4，R2选自氢，取代或未取代的1至6个碳原子的烷基和无毒，药学上可接受的矿物质的阳离子 和有机碱，其制备方法和新型中间体。 式I化合物具有止痛和抗炎特性。

    1-oxa-a-nor-steroids
    32.
    发明授权
    1-oxa-a-nor-steroids 失效
    1-OXA-A-NOR-STEROIDS

    公开(公告)号：US3676461A

    公开(公告)日：1972-07-11

    申请号：US3676461D

    申请日：1969-07-07

    Applicant: ROUSSEL UCLAF

    Inventor： MULLER GEORGES ,  BARDONESCHI ROLAND

    IPC: C07D303/32 ,  C07D303/40 ,  C07J73/00 ,  C07D5/34

    CPC classification number: C07J73/003 ,  C07C2603/16 ,  C07D303/32 ,  C07D303/40

    Abstract: 1-Oxa-13 Beta -R1-17 Alpha -methyl-A-nor- Delta 3(5),9gonadienes of the formula

    WHEREIN R1 is alkyl of one to three carbon atoms and R2 is acyl of an aliphatic carboxylic acid of two to four carbon atoms having antiandrogenic activity and their preparation and intermediates formed therein.

    Abstract translation: 1-氧杂-13β-1R-17α-甲基-α-去甲-TATA 3（5），9-式：其中R 1是具有1至3个碳原子的烷基，R 2是脂族羧酸的酰基， 二至四个具有抗雄激素活性的碳原子及其制备和其中形成的中间体。

    17alpha 21 alkenylidene dioxy derivatives of pregnane and process for preparation thereof
    33.
    发明授权
    17alpha 21 alkenylidene dioxy derivatives of pregnane and process for preparation thereof 失效
    17ALPHA 21阿魏酸二恶英衍生物及其制备方法

    公开(公告)号：US3651049A

    公开(公告)日：1972-03-21

    申请号：US3651049D

    申请日：1970-03-12

    Applicant: ROUSSEL UCLAF

    Inventor： BOISSIER JACQUES R ,  RATOUIS ROGER

    IPC: A61K31/573 ,  A61K31/58 ,  C07D319/08 ,  C07J21/00 ,  C07C173/00

    CPC classification number: A61K31/573 ,  A61K31/58 ,  C07D319/08 ,  C07J21/00

    Abstract: CYCLIC ACETAL DERIVATIVES OF PREGNANE OF GENERAL FORMULA:

    3,5''-DI(O=),6-Z,9-Y,16-P,2''-(R1-CH=C(-R)-(CH2)N-)SPIRO

    (ANDROSTA-1,4-DIENE-17,4''-(1,3)DIOXANE) WITH X IN

    POSITION 11

    WHEREIN X:CO OR CH2 OR CHOH-Y:H OR F-Z:H OR CH3-P:H OR ALKYL OR ALKYIDENE-N: O OR 1-R:H OR HALOGEN OR ALKYL-R1:H OR ALKYL OR CARBOXYL OR ALKOXYCARBONYL-BROKEN LINE IN THE RING A: OPTIONAL PRESENCE OF A DOUBLE BOND. THESE PRODUCTS ARE VERY USEFUL SUBSTANCES IN HUMAN AND ANIMAL THERAPY, ESPECIALLY OWING TO THEIR REMARKABLE ANTI-INFLAMMATORY ACTION. THE PRODUCTS ARE PREPARED BY ACTION OF A DIALKYL ACETAL ON A PREGNANE DERIVATIVE HAVING HYDROXYL RADICALS IN ITS 17 AND 21 POSITIONS, IN THE PRESENCE OF AN ACID CATALYST.

    Benzimidazole derivatives of benzoic acid and its esters and amides
    35.
    发明授权
    Benzimidazole derivatives of benzoic acid and its esters and amides 失效
    苯甲酸的苯并咪唑衍生物及其酯及其衍生物

    公开(公告)号：US3644382A

    公开(公告)日：1972-02-22

    申请号：US3644382D

    申请日：1969-03-18

    Applicant: ROUSSEL UCLAF

    Inventor： CLEMENCE FRANCOIS ,  MARTRET ODILE LE

    IPC: C07D213/82 ,  C07D235/06 ,  C07D235/08 ,  C07D235/18 ,  C07D307/68 ,  C07D333/38 ,  C07D49/38

    CPC classification number: C07D213/82 ,  C07D235/06 ,  C07D235/08 ,  C07D235/18 ,  C07D307/68 ,  C07D333/38

    Abstract: BENZIMIDAZOLES OF THE FORMULA

    1-(2-R-PHENYL),2-R1,5-X'',6-X-BENZMIDAZOLE

    WHERIN X AND X'' MAY BE DIFFERENT AND ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, HALOGEN, ALKYL, ALKOXY, TRIHALOMETHYL AND NITRO, R IS SELECTED FROM THE GROUP CONSISTING OF -COOH, -COOR'', AND

    -CO-N(-A)-B

    R'' IS SELECTED FROM THE GROUP CONSISTING OF ALIPHATIC AND HHDROXYLATED RESIDUE OF A GLYCOL, A AND B ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN AND OPTIONALLY SUBSTITUTED ALIPHATIC AND R1 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, LOWER ALIPHATIC HDROCARBON, UNSUBSTITUTED AND POLYSUBSTITUTED ARYL, ARYLALIPHATIC, A THIENYL, A B-PYRIDYL AND A FURYL WITH THE PROVISO THAT WHEN R1 IS PHENYL, X'' AND X ARE OTHER THAN HALOGEN, ALKOXY AND TRIFLUROMETHYL WHICH COMPOUNDS POSSESS ANTI-INFLAMMATORY AND ANTIVIRAL ACTIVITY AND A NOVEL PROCESS FOR THEIR PREPARATION.

    3-amino-4-dihalo pyrazolones
    36.
    发明授权
    3-amino-4-dihalo pyrazolones 失效
    3-氨基-4-二氢吡喃酮

    公开(公告)号：US3632818A

    公开(公告)日：1972-01-04

    申请号：US3632818D

    申请日：1969-01-02

    Applicant: ROUSSEL UCLAF

    Inventor： ALLAIS ANDRE ,  GIRAULT PIERRE

    IPC: A01N43/56 ,  C07D231/52 ,  C07D49/06

    CPC classification number: C07C243/00 ,  C07D231/52

    Abstract: 3-AMINO-4,4-DIHALO-5-PYRAZOLONES OF THE FORMULA

    1-Y,3-(R-N(-R1)-),4-X,4-X'',5-(O=)-2-PYRAZOLINE

    WHEREIN X AND X'' ARE SELECTED FRO THE GROUP CONSISTING OF CHLORINE AND BROMINE, Y IS SELECTED FROM THE GROUP CONSISTING OF ALKYL, CYCLOALKYL, AND ARYL WHICH MAY BE SUBSTITUTED AND R AND R1 ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, ALKYL, ARYL, CYCLOALKYL AND ARALKYL WHICH POSSES; FUNGICIDAL ACTIVITY AND THEIR PREPARATION.

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