HRID1363823

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID21455623

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

C7H10N2O2S2

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

HCID57668194

未命名化合物

HCID66962180

1-{6-[(Cyclopentylmethyl)amino]-2,3-dihydro-1H-indol-1-yl}ethan-1-one

C16H22N2O

结构：CCOC(=O)CSc1cnc(NC(=O)N(CC2CCCC2)c2ccc3c(c2)N(C(C)=O)CC3)s1

HCID86629949

未命名化合物

PRODUCTS

生成物

结构：CC(=O)N1CCc2ccc(N(CC3CCCC3)C(=O)Nc3ncc(SCC(=O)O)s3)cc21

HCID57668235

未命名化合物

PROCEDURE

实验过程

The title compound was prepared via {2-[3-(1-acetyl-2,3-dihydro-1H-indol-6-yl)-3-cyclopentylmethyl-ureido]-thiazol-5-ylsulfanyl}-acetic 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 1-[6-(cyclopentylmethyl-amino)-2,3-dihydro-indol-1-yl]-ethanone and (2-amino-thiazol-5-ylsulfanyl)acetic acid ethyl ester

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-2e2c2274273b427397f0e4be4ce47879
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:34])[CH2:5][S:6][C:7]1[S:11][C:10]([NH:12][C:13]([N:15]([C:22]2[CH:30]=[C:29]3[C:25]([CH2:26][CH2:27][N:28]3[C:31](=[O:33])[CH3:32])=[CH:24][CH:23]=2)[CH2:16][CH:17]2[CH2:21][CH2:20][CH2:19][CH2:18]2)=[O:14])=[N:9][CH:8]=1)C.C1(CN(C2C=CC(S(C)(=O)=O)=CC=2)C(=O)NC2SC=C(CC(O)=O)N=2)CCCC1.C1(CNC2C=C3C(CCN3C(=O)C)=CC=2)CCCC1.C(OC(=O)CSC1SC(N)=NC=1)C>>[C:31]([N:28]1[C:29]2[C:25](=[CH:24][CH:23]=[C:22]([N:15]([CH2:16][CH:17]3[CH2:21][CH2:20][CH2:19][CH2:18]3)[C:13](=[O:14])[NH:12][C:10]3[S:11][C:7]([S:6][CH2:5][C:4]([OH:34])=[O:3])=[CH:8][N:9]=3)[CH:30]=2)[CH2:26][CH2:27]1)(=[O:33])[CH3:32]