CAS: 81870-64-6; ((Chloromethyl)Phenylethyl)Methyldichlorosilane

该化合物是一种氯化有机硅化合物,具有硅-氯和苯-氯功能组,其双功能再活性在有机硅合成中具有价值,特别是作为交叉关联剂或表面修饰剂的前体.氯甲基苯基混合物能够进一步衍生,而二氯硅类则有利于水解或凝聚反应,使其在硅酮聚合物和混合材料应用中有用.该化合物由于其定义明确的结构,在粘合反应方面提供了精确的控制,确保了硅酮特殊配方的一贯性.由于水分敏度和潜在腐蚀性,需要谨慎处理.

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    专利信息


    专利号:US-7189864-B2
    优先权日:1990-11-19
    标 题:Method of preparing intermediates useful in synthesis of retroviral protease inhibitors
    发明人:NG JOHN S; PRZYBYLA CLAIRE A; MUELLER RICHARD A; VAZQUEZ MICHAEL L; GETMAN DANIEL P
    权利人:SEARLE & CO
    摘要:A synthesis is described for intermediates which are readily amenable to the large scale preparation of hydroxyethylurea-based chiral HIV protease inhibitors. The method includes forming a diastereoselective epoxide from a chiral alpha amino aldehyde.

    专利号:US-6022996-A
    优先权日:1990-11-19
    标 题 :Method for making intermediates useful in synthesis of retroviral protease inhibitors
    发明人:NG JOHN S; PRZYBYLA CLAIRE A; MUELLER RICHARD A; VAZQUEZ MICHAEL L; GETMAN DANIEL P
    权利人:SEARLE & CO
    摘要:A synthesis is described for intermediates which are readily amenable to the large scale preparation of hydroxyethylurea-based chiral HIV protease inhibitors. The method includes forming a diastereoselective epoxide from a chiral alpha amino aldehyde.

    专利号:EP-0641333-B1
    优先权日:1992-05-20
    标 题 :Method for making intermediates useful in synthesis of retroviral protease inhibitors
    发明人:NG JOHN S; PRZYBYLA CLAIRE A; MUELLER RICHARD A; VAZQUEZ MICHAEL L; GETMAN DANIEL P
    权利人:SEARLE & CO; MONSANTO CO
    摘要:A synthesis is described for intermediates which are readily amenable to the large scale preparation of hydroxyethylurea-based chiral HIV protease inhibitors. The method includes forming a diastereoselective epoxide compound of formula (I) from a chiral alpha amino aldehyde and halomethyllithium as an organometallic methylene-adding reagent. In formula (I) R<1> is selected from alkyl, aryl, cycloalkyl, cycloalkylalkyl and arylalkyl, which are optionally substituted with a group selected from alkyl, halogen, NO2, OR<9> or SR<9>, where R<9> represents hydrogen or alkyl; and P<1> and P<2> independently are selected from amine protecting groups, including but not limited to, arylalkyl, substituted arylalkyl, cycloalkenylalkyl and substituted cycloalkenylalkyl, allyl, substituted allyl, acyl, alkoxycarbonyl, aralkoxycarbonyl and silyl.

    专利号:EP-0855388-B1
    优先权日:1993-11-23
    标 题 :Method for making intermediates useful in synthesis of retroviral protease inhibitors
    发明人:NG JOHN S; PRZYBYLA CLAIRE A; MUELLER RICHARD A; VAZQUEZ MICHAEL L; GETMAN DANIEL P; FRESKOS JOHN J; DECRESCENZO GARY A; BERTENSHAW DEBORAH E; HEINTZ ROBERT M; ZHANG SUHONG; LIU CHIN; LANEMAN SCOTT A
    权利人:SEARLE & CO
    摘要:A synthesis is described for intermediates which are readily amenable to the large scale preparation of hydroxyethylurea-based chiral HIV protease inhibitors. The method includes forming a cyanohydrin from a chiral alpha amino aldehyde.

    专利号:US-5872299-A
    优先权日:1990-11-19
    标 题 :Method of preparing intermediates for retroviral protease inhibitors
    发明人:NG JOHN S; PRZYBYLA CLAIRE A; MUELLER RICHARD A; VAZQUEZ MICHAEL L; GETMAN DANIEL P; FRESKOS JOHN J; DECRESCENZO GARY A; BERTENSHAW DEBORAH E; HEINTZ ROBERT M; ZHANG SUHONG; LIU CHIN; LANEMAN SCOTT A
    权利人:SEARLE & CO
    摘要:A synthesis is described for intermediates which are readily amenable to the large scale preparation of hydroxyethylurea-based chiral HIV protease inhibitors. The method includes forming a diastereoselective epoxide or cyanohydrin from a chiral alpha amino aldehyde.

    专利号:US-2005171366-A1
    优先权日:1990-11-19
    标 题 :Method of preparing intermediates useful in synthesis of retroviral protease inhibitors

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