CAS: 78603-93-7; (R)-2-Amino-1,1-Diphenylpropan-1-Ol

该化合物是有机化合物,其特点是其个性结构,包括一个氨基组和两个联苯组,附于丙诺基骨骨中,该化合物一般是白色的,以其在非对称合成中,特别是在制药生产中作为手性辅助剂的作用著称,其立体化学学允许它有选择地与其他手性分子相互作用,使其在对应选择性反应中具有价值.氨基组的存在有助于氢联结的本质和潜力,影响其溶剂中的溶解性和再活性.此外,二苯基结构增强了其稳定性,并可能影响其物理特性,例如熔点和沸点.

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欧盟法规

ECHA物质C&L通报

上下游产品

D-alanine methyl ester hydr°Chloride 2-amino-1,1-diphenyl-1-propanol phenylmagnesium bromide bromobenzene naphthalene-1-sulfonic acid ((R)-2-hydroxy-1-methyl-2,2-diphenyl-ethyl)-amide

合成工艺路线路线简述

    📜Alkaline Earth Salt Of/the/ Methylsulfuric Acid置于camphor-10-Sulfonic Acid体系中,化学反应生成 (R)-(+)-2-氨基-1,1-二苯基-1-丙醇
    参考文献:Molecular Rearrangements. Xi. The Deamination Of 1,1-Diphenyl-2-Amino-1-Propanol1
    标题:Molecular Rearrangements. Xi. The Deamination Of 1,1-Diphenyl-2-Amino-1-Propanol1
    摘要:
    DOI:10.1021/ja01580A015

    海关参考信息

    专利信息


    专利号:US-2013253061-A1
    优先权日:2012-03-20
    标 题:Method of droxidopa synthesis
    发明人:PIMPLASKAR HARISH K; KADAM SHASHIKANT VITHAL; MALLESH VOORADI; KAWALE PRAMOD MANGALDAS
    权利人:CHELSEA THERAPEUTICS INC
    摘要:The present application relates to a novel method of preparing L-threo-dihydroxyphenylserine (droxidopa). Specifically, the application is directed to a method of preparing droxidopa via a deprotection step that is an alternative to deprotection steps that have been previously disclosed. The new deprotection strategy is advantageous in that it avoids the need to use hydrogenolysis or hydrazine.

    专利号:WO-2013142093-A1
    优先权日:2012-03-20
    标题 :Method for the synthesis of droxidopa

    专利号:US-4480109-A
    优先权日:1982-01-14
    标 题:Process for producing threo-3-(3,4-dihydroxyphenyl)serine
    发明人:OHASHI NAOHITO; NAGATA SHOJI; ISHIZUMI KIKUO
    权利人:SUMITOMO CHEMICAL CO
    摘要:A process for producing an optically active threo-3-(3,4-dihydroxyphenyl)serine represented by the formula ##STR1## which is useful as a remedy for peripheral orthostatic hypotension or as an antidepressant, which process comprises treating threo-3-(3,4-methylenedioxyphenyl)serine or an N-carbobenzoxy derivative thereof represented by the formula ##STR2## wherein A represents a hydrogen atom or a carbobenzoxy group, with a Lewis acid to form threo-3-(3,4-dihydroxyphenyl)serine or an N-carbobenzoxy derivative thereof represented by the formula ##STR3## wherein A is as defined above, and, if A is a carbobenzoxy group, catalytically reducing the resulting compound of formula [2]; a racemic or optically active threo-N-carbobenzoxy-3-(3,4-methylenedioxyphenyl)serine represented by the formula ##STR4## which is a novel compound useful as an intermediate in the above synthesis; and a process for producing said novel compound.

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