HRID1881066

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2725062

2-Chloro-4-fluorobenzyl bromide

C7H5BrClF

HCID57481427

Ethyl 2-[(2-amino-1,3-thiazol-5-yl)sulfanyl]-2-methylpropanoate

C9H14N2O2S2

结构：CC(C)(CSc1cnc(NC(=O)N(CCOCc2ccccc2Cl)[C@H]2CC[C@H](C)CC2)s1)C(=O)O

HCID178454946

未命名化合物

PRODUCTS

生成物

结构：CC(C)(Sc1cnc(NC(=O)N(CCOCc2ccc(F)cc2Cl)[C@H]2CC[C@H](C)CC2)s1)C(=O)O

HCID178460773

未命名化合物

PROCEDURE

实验过程

The compound was prepared following an analogous procedure to the one described for the synthesis of 3-{2-[3-[2-(2-chloro-benzyloxy)-ethyl]-3-(trans-4-methyl -cyclohexyl)-ureido]-thiazol-5-ylsulfanyl}-2,2-dimethyl-propionic acid using 1-bromomethyl-2-chloro-4-fluoro-benzene and 2-(2-amino-thiazol-5-ylsulfanyl)-2-methyl-propionic acid ethyl ester.

WORKUP

后处理

customThe compound was prepared