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HRID1810061

反应详情

EQUATION

反应方程式

HRID 1810061 的结构方程式

REACTANTS

反应物

3
结构：BrCCc1ccccc1
HCID7666

Phenethyl bromide

C8H9Br

结构：CC(C)(Sc1cnc(NC(=O)N(CCc2ccccc2)[C@H]2CC[C@H](C)CC2)s1)C(=O)O
HCID178460750

未命名化合物

结构：CO[C@H]1CC[C@H](N)CC1
HCID178496609

未命名化合物

PRODUCTS

生成物

1
结构：CO[C@H]1CC[C@H](N(CCc2ccccc2)C(=O)Nc2ncc(SCC(=O)O)s2)CC1
HCID178496612

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

1
结构：CCOC(C)=O
溶剂HCID8857

Ethyl acetate

C4H8O2

PROCEDURE

实验过程

The compound was prepared following an analogous procedure to the one described for the synthesis of 2-methyl-2-{2-[3-(trans-4-methyl-cyclohexyl)-3-phenethyl-ureido]-thiazol-5-ylsulfanyl}-propionic acid using trans-4-methoxy-cyclohexylamine (prepared as described in J. Med. Chem. 1977, 20, 279-290), 2-phenylethylbromide and 2-aminothiazol-5-ylsulfanyl)acetic acid ethyl ester.

WORKUP

后处理

  1. customThe compound was prepared