Method of tranquilizing animals
    2.
    发明授权
    Method of tranquilizing animals 失效
    镇静动物的方法

    公开(公告)号:US3879524A

    公开(公告)日:1975-04-22

    申请号:US31207872

    申请日:1972-12-04

    摘要: WHERE R2 is hydrogen, chloro- or dimethylamino-.

    WHERE X is -O- or -S-, R and R1 are hydrogen, methyl or hydroxymethyl and are the same or different, and Z is methyl, ethyl, methoxymethyl, p-methoxyphenyl; or 4,4-dimethyl-2oxazolylethyl; 4,4-dimethyl-2-oxazolylbutyl; or the group

    A method of tranquilizing warm-blooded animals comprising administering thereto orally or intravenously a tranquilizing amount of a compound, or a phramaceutically acceptable salt thereof, corresponding to the formula

    摘要翻译: 一种镇静温血动物的方法,其包括口服给药或静脉内给药一定量的化合物或其药物上可接受的盐,其对应于式X-O-或-S-,R和R 1为氢,甲基 或羟甲基并且相同或不同,Z是甲基,乙基,甲氧基甲基,对甲氧基苯基; 或4,4-二甲基-2-恶唑基乙基; 4,4-二甲基-2-恶唑基丁基; 或者其中R 2是氢,氯或二甲基氨基。

    Tranquilizers
    3.
    发明授权
    Tranquilizers 失效
    TRANQUILIZERS

    公开(公告)号:US3876770A

    公开(公告)日:1975-04-08

    申请号:US45692874

    申请日:1974-04-01

    IPC分类号: A61K31/42 A61K27/00

    CPC分类号: A61K31/42

    摘要: Tranquilizing agents for warm-blooded animals corresponding to the formula

    Where n can be 1 or 2; Y can be --(CH.sub.2).sub.n -- or

    Where R.sup.2 can be hydrogen or an alkyl, alkenyl, alkoxy, phenyl or methoxyphenyl radical. Z can be thenyl, furyl, phenyl; or mono-, di-, or trimethoxyphenyl, mono-, or dichlorophenyl, or dichlorophenoxy. R and R.sup.1 can be hydrogen, methyl, or ethyl and can be the same or different.

    Synthesis of zearalanes ii and related compounds and intermediates useful in the syntheses thereof
    4.
    发明授权
    Synthesis of zearalanes ii and related compounds and intermediates useful in the syntheses thereof 失效
    ZEARALANES II及相关化合物的合成及其合成中的有用之作用

    公开(公告)号:US3836544A

    公开(公告)日:1974-09-17

    申请号:US24728272

    申请日:1972-04-25

    发明人: URRY W MULLENBACH G

    摘要: THIS INVENTION PROVIDES A NEW SYNTHESIS FOR NORZEARALANE II AND RELATED COMPOUNDS WHICH RELATED COMPOUNDS AND NORZEARALANE II ARE REPRESENTED BY THE FORMULA

    1,5-DI(HO-),2,3-(-CO-O-CH2-(CH2)X-)-BENZENE

    WHERE X IS AN INTEGER HAVING A VALUE FROM 1 TO 13 INCLUSIVE. THE ANABOLIC AGENT NORZEARALANE II, IN WHICH X=9 IN THEFOREGOING FORMULA, IS PREPARED BY A TOTAL CHEMICAL SYNTHESIS INVOLVING THE REACTION OF 10-UNDECENAL WITH MALONIC ACID TO PRODUCE TRANS-2,12-TRIDECADIENOIC ACID; TREATING THE ACID SO FORMED WITH DIAZOMSTHANE TO YIELD METHYL TRANS-2,12-TRIDECADIENOATE; REACTING THE METHYL ESTER WITH ETHYL ACETOACETATE AND SODIUM ETHOXIDE TO FORM THE SODIUM SALT OF ETHYL 6-(9-DECENYL)-B-DIHYDRORESORCYLATE; BROMINATING THE DIHYDRORESORCYLATE TO PREPARE ETHYL 3-BROMO- 6 - (9-DECENYL)-B-DIHYDRORESOCRYLATE; DE-HYDROBROMINATING THE FOREGOING BROMO DERIVATIVE TO GIVE ETHYL 6-(9-DECENYL)-B-RESORCYLATE; REACTING THE RESORCYLATE ESTER WITH BENZYL CHLORIDE TO PRODUCE ETHYL 6-(9-DECENYL)-BRESORCYLATE DIBENZYL ETHER; SUBJECTING THE BENZYLATED ESTER TO THE ACTION OF DIBORANE, WATER AND HYDROGEN PEROXIDE TO FORM ETHYL 2,4-BIS (BENZYLOXY)-6-(10-HYDROXYDECYL)BENZOATE; TREATING THE FOREGOING BENZOATE WITH SODIUM ETHOXIDE TO PREPARE NORZEARALANE II DIBENZYL ETHER, ONE ALSO TO PREPARE AS A BY-PRODUCT THE DIMERIC DILACTONE OF 2,4-BIS(BENZYLOXY)-6-(10-HYDROXYDECYL)-BENZOIC ACID; HYDROGENATING NORZEARALANE II DIBENZYL ETHER TO FORM NORZEARALANE II. IN GENERAL, A HOMOLOGUE OF NORZEARALANE II AND/OR OF THE CORRESPONDING DIMERIC DILACTONE IS PREPARED BY SUBSTITUTING FOOR 10-UNDECENAL IN THE FOREGOING SEQUENCE OF REACTIONS AN UNSATURATED ALDEHYDE HAVING THE FORMULA

    CH2=CH-(CH2)X-1-CHO

    WHERE X IS AN INTEGER WHICH MAY HAVE THE VALUE 1,2,3,4, 5, 6, 7, 8, 9, 10, 11, 12 OR 13 SPECIFICALLY ZEARALANE II (WHERE X=10) IS PREPARED STARTING WITH 11-DODECENAL AND THE DIMERIC DILACTONE FROM 6-(5-HYDROXYPENTYL-B-RESORCYCLIC ACID DIBENZYL ETHER IS PREPARED WHEN THE STARTING ALDEHYDE IS 5-HEXENAL (WHERE X= 4) THE INVENTION ALSO COVERS PHYSIOLOGICALLY ACTIVE COMPOUNDS RELATED TO THE ZEARALANES II AND KNOW AS DIMERIC DILACTONES HAVING THE FORMULA,

    1,5-DI(RO-),2,3-(-CO-O-CH2-(CH2)X-(3,5-DI(RO-)-1,6-PHENYL

    ENE)-CO-O-CH2-(CH2)X-)-BENZENE

    X IS AN INTEGER WHICH MAY HAVE THE VALUE 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 OR 13 AND WHERE R IS EITHE HYDROGEN OR A BENZYL RADICAL (C6H5CH2-). MORE PARTICULARLY, THIS INVENTION RELATES TO NOVEL INTERMEDIATES PRODUCED IN THE SYNTHESIS OF THE ABOVE COMPOUNDS AND TO PROCESSES FOR MAKING THESE INTERMEDIATES.

    Method of administering cycloserine
    5.
    发明授权
    Method of administering cycloserine 失效
    施用环磷酰胺的方法

    公开(公告)号:US3821392A

    公开(公告)日:1974-06-28

    申请号:US34266473

    申请日:1973-03-19

    发明人: HARNED R

    IPC分类号: A61K31/42 A61K27/00

    CPC分类号: A61K31/42

    摘要: A method of administering cycloserine to an animal for prophylactic or therapeutic purposes by metering a concentrated alkaline solution of cycloserine into the drinking water provided for the animal in an amount sufficient to provide an effective dosage.

    Method for coating steel
    7.
    发明授权
    Method for coating steel 失效
    涂钢方法

    公开(公告)号:US3783002A

    公开(公告)日:1974-01-01

    申请号:US3783002D

    申请日:1972-01-14

    发明人: PURCELL R SAUSAMAN D

    IPC分类号: B05D7/16 B32B15/08 B44D1/36

    CPC分类号: B05D7/16

    摘要: A PROCESS FOR COATING STEEL BY APPLYING THERETO A MONOMER OR PARTIAL POLYMER OF A VINYL OXAZOLINE, REPRESENTED BY THE FORMULA

    2-(CH2=C(-R)-),4-R1,4-R2-2-OXAZOLINE

    WHEREIN R IS AN ALKYL OR ALKENYL GROUP OF 1 TO 20 CARBON STOMS AND R1 AND R2 ARE SELECTED FROM THE GROUP CONSISTIG OF METHYL, ETHYL, HYDROXYMETHYL, OR THE ACYLOXYMETHYL GROUP REPRESENTED BY THE FORMULA

    -CH2-OOC-CH2-R

    OR THE VINYL ACYLOXYMETHYL GROUP REPRESENTED BY THE FORMULA

    -CH2-OOC-C(-R)=CH2

    HEATING TO EFFECT FURTHER POLYMERIZATION, APPLYING THERETO A SOLUTION OR DISPERSION OF A VINYL HALIDE POLYMER, COPOLYMER, OR TERPOLYMER AND HEATING TO EFFECT EVAPORATION OF THE SOLVENT OR COALESCENE OF THE DISPERSION.

    F.e.s. derivatives
    8.
    发明授权
    F.e.s. derivatives 失效
    美国 衍生物

    公开(公告)号:US3764614A

    公开(公告)日:1973-10-09

    申请号:US3764614D

    申请日:1970-02-16

    发明人: WEHRMEISTER H URRY W

    摘要: New compounds are provided and have the formula

    WHERE B is

    R and R'' can be hydrogen, alkyl, acyl or aralkyl radicals; and X and Y are hydrogen or chlorine and at least one of X and Y is chlorine. These compounds exhibit antibacterial activity and can be used in animal feed compositions.

    摘要翻译: 提供新的化合物,其结构式为WHERE B是R,R'可以是氢,烷基,酰基或芳烷基; X和Y是氢或氯,X和Y中的至少一个是氯。 这些化合物表现出抗菌活性并可用于动物饲料组合物。

    Water-soluble alkyd resin compositions
    10.
    发明授权
    Water-soluble alkyd resin compositions 失效
    水溶性烷基树脂组合物

    公开(公告)号:US3699065A

    公开(公告)日:1972-10-17

    申请号:US3699065D

    申请日:1971-03-04

    发明人: CLARK EDGAR L

    CPC分类号: C08G63/46 Y10S524/901

    摘要: A WATER-SOLUBLE ALKYL RESIN COMPOSITION AND A 2-STEP PROCESS FOR THE PREPARATION THEREOF COMPRISING THE PRODUCT OF THE REACTION OF AN ALIPHATIC MONOCARBOXYLIC ACID WITH DI- OR TRIPENTAERYTHRITOL, WHICH PRODUCT IS THEN REACTED WITH PHTHALIC ANHYDRIDE TO AN ACID NUMBER OF 70-100, THEN NEUTRALIZED. THE COMPOSITION IS USEFUL IN THE FORMULATION OF PROTECTIVE COATINGS, ESPECIALLY THOSE INTENDED FOR APPLICATION BY THE ELECTRO-DEPOSITION PROCESS.