HRID1363753

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID43453307

N-(Cyclopentylmethyl)-4-(methanesulfonyl)aniline

C13H19NO2S

HCID57481428

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

C8H12N2O2S2

结构：CS(=O)(=O)c1ccc(N(CC2CCCC2)C(=O)Nc2nc(CC(=O)O)cs2)cc1

HCID57668194

未命名化合物

结构：CCOC(=O)CCSc1cnc(NC(=O)N(CC2CCCC2)c2ccc(S(C)(=O)=O)cc2)s1

HCID86629886

未命名化合物

PRODUCTS

生成物

结构：CS(=O)(=O)c1ccc(N(CC2CCCC2)C(=O)Nc2ncc(SCCC(=O)O)s2)cc1

HCID57668382

未命名化合物

PROCEDURE

实验过程

The title compound was prepared via 3-{2-[3-cyclopentylmethyl-3-(4-methanesulfonyl-phenyl)-ureido]-thiazol-5-ylsulfanyl}-propionic acid ethyl ester in a similar manner as described for the synthesis of {2-[3-cyclopentylmethyl-3-(4-methanesulfonyl-phenyl)-ureido]-thiazol-4-yl}-acetic acid, using cyclopentylmethyl-(4-methanesulfonyl-phenyl)-amine and 3-(2-amino-thiazol-5-ylsulfanyl)-propionic acid ethyl ester.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-aaf0b633ff0b4b8695bc582c0f21aefc
来源数据集: uspto-grants-2011_02
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07884210B2
来源说明: uspto-grants-2011_02

反应 SMILES

C([O:3][C:4](=[O:33])[CH2:5][CH2:6][S:7][C:8]1[S:12][C:11]([NH:13][C:14]([N:16]([CH2:27][CH:28]2[CH2:32][CH2:31][CH2:30][CH2:29]2)[C:17]2[CH:22]=[CH:21][C:20]([S:23]([CH3:26])(=[O:25])=[O:24])=[CH:19][CH:18]=2)=[O:15])=[N:10][CH:9]=1)C.C1(CN(C2C=CC(S(C)(=O)=O)=CC=2)C(=O)NC2SC=C(CC(O)=O)N=2)CCCC1.C1(CNC2C=CC(S(C)(=O)=O)=CC=2)CCCC1.C(OC(=O)CCSC1SC(N)=NC=1)C>>[CH:28]1([CH2:27][N:16]([C:17]2[CH:22]=[CH:21][C:20]([S:23]([CH3:26])(=[O:24])=[O:25])=[CH:19][CH:18]=2)[C:14](=[O:15])[NH:13][C:11]2[S:12][C:8]([S:7][CH2:6][CH2:5][C:4]([OH:33])=[O:3])=[CH:9][N:10]=2)[CH2:32][CH2:31][CH2:30][CH2:29]1