HRID1581917

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID3717105

Ethanesulfonate

C2H5O3S-

结构：C[C@@H](NC(=O)c1cnc2cc(NC(=O)c3ccccc3-c3ccc(C(F)(F)F)cc3)ccc2c1)c1ccccc1

HCID70230681

未命名化合物

PRODUCTS

生成物

结构：CCC(NC(=O)c1cnc2cc(NC(=O)c3ccccc3-c3ccc(C(F)(F)F)cc3)ccc2c1)c1ccccc1

HCID10146397

未命名化合物

PROCEDURE

实验过程

(R)-7-[(4′-trifluoromethyl-biphenyl-2-carbonyl)-amino]-quinoline-3-carboxylic acid (1-phenyl-ethyl)-amide, ethanesulfonate;

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-86ac01394e91412487533e63f5330a34
来源数据集: uspto-grants-2004_05
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06734175B2
来源说明: uspto-grants-2004_05

反应 SMILES

[C:1]1([C@H:7]([NH:9][C:10]([C:12]2[CH:13]=[N:14][C:15]3[C:20]([CH:21]=2)=[CH:19][CH:18]=[C:17]([NH:22][C:23]([C:25]2[C:26]([C:31]4[CH:36]=[CH:35][C:34]([C:37]([F:40])([F:39])[F:38])=[CH:33][CH:32]=4)=[CH:27][CH:28]=[CH:29][CH:30]=2)=[O:24])[CH:16]=3)=[O:11])[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:41](S([O-])(=O)=O)C>>[C:1]1([CH:7]([NH:9][C:10]([C:12]2[CH:13]=[N:14][C:15]3[C:20]([CH:21]=2)=[CH:19][CH:18]=[C:17]([NH:22][C:23]([C:25]2[C:26]([C:31]4[CH:32]=[CH:33][C:34]([C:37]([F:40])([F:38])[F:39])=[CH:35][CH:36]=4)=[CH:27][CH:28]=[CH:29][CH:30]=2)=[O:24])[CH:16]=3)=[O:11])[CH2:8][CH3:41])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1