CAS: 1320-51-0; Urea, N-(Hydroxyethyl)-

该化合物是一种有机化合物,其特征是尿素和氢氧乙基功能组,通常看起来像是白色晶状固体或粉末,由于其极性,在水中可以溶解,众所周知,该化合物具有割除功能,这意味着它可以保持水分,使其在各种化妆品和药剂配方中具有价值.此外,(乙基)尿素可以作为合成其他化学化合物的建筑块,并经常用于研究环境,其化学结构允许氢结合,有助于其溶解性以及与生物系统的互动.安全数据表明,虽然一般认为氢的毒性较低,但应当遵守适当的处理和安全措施,以尽量减少接触.

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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:CN-103497215-B
    优先权日:2007-12-18
    标题 :Reagents and methods for the synthesis of beta-ketoamide as a precursor to the synthesis of immune adjuvant E6020

    专利号:CN-102149675-A
    优先权日:2007-12-18
    标题:Reagents and methods for the synthesis of beta-ketoamide as a precursor to the synthesis of immune adjuvant E6020

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    摘要:International Journal of Toxicology 43(Suppl. 3):128S-134S, 2024
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