L-亮氨酸乙酯 → HCID 131719291，化合物

HRID 1440074

反应方程式

HRID 1440074 反应方程式
[C:1]([S:4][CH2:5][CH:6]([CH2:10][CH:11]([CH3:13])[CH3:12])[C:7](Cl)=[O:8])(=[O:3])[CH3:2].[NH2:14][C@H:15]([C:20]([O:22][CH2:23][CH3:24])=[O:21])[CH2:16][CH:17]([CH3:19])[CH3:18].C(N(C(C)C)CC)(C)C>C(Cl)Cl>[C:1]([S:4][CH2:5][CH:6]([CH2:10][CH:11]([CH3:13])[CH3:12])[C:7]([NH:14][C@H:15]([C:20]([O:22][CH2:23][CH3:24])=[O:21])[CH2:16][CH:17]([CH3:19])[CH3:18])=[O:8])(=[O:3])[CH3:2]

参与物

5

反应物 3

HCID 75971L-亮氨酸乙酯HCID 81531N,N-二异丙基乙胺HCID 127690742-[(Acetylthio)methyl]-4-methylpentanoyl chloride

产物 1

HCID 131719291HCID 131719291，化合物

试剂、催化剂与溶剂 1

HCID 6344二氯甲烷溶剂

实验过程

2-Acetylthiomethyl-4-methylpentanoyl chloride and (L)-leucine, ethyl ester are reacted in methylene chloride in the presence of diisopropylethylamine at a temperature below 0° according to the procedure of Example 26 to yield (±)-N-[2-(acetylthiomethyl)-4-methyl-1-oxopentyl]-L-leucine, ethyl ester.

来源与证据

ORD记录
ord-5431d0014d5a41f09bda713037b05564
来源数据集
uspto-grants-1996_03
专利号
US05496805

关联笔记

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