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【结 构 式】

【分子编号】37944

【品名】1-methylhexylamine; 2-heptanamine

【CA登记号】123-82-0

【 分 子 式 】C7H17N

【 分 子 量 】115.21872

【元素组成】C 72.97% H 14.87% N 12.16%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(III)

For the synthesis of the optically pure (R)-enantiomer, racemic 2-heptylamine (III) was resolved by means of immobilized, recombinant Candida antarctica lipase. The required (R)-2-heptylamine (IV) was then converted to the title compound by sequential methylation and propargylation.

1 Berry, M.D.; R-2HMP: An orally active agent combining independent antiapoptotic and MAO-B-inhibitory activities. CNS Drug Rev 1999, 5, 2, 105.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(III) 37944 1-methylhexylamine; 2-heptanamine 123-82-0 C7H17N 详情 详情
(IV) 37945 (2R)-2-heptanamine; (1R)-1-methylhexylamine 6240-90-0 C7H17N 详情 详情
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