HRID446865

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2737250

1-(2-pyrrolidin-1-ylethyl)piperazine

C10H21N3

结构：O=C(O)CNC(=O)c1ccc(S(=O)(=O)Nc2ccccc2C(=O)c2ccccc2)cc1

HCID68494538

未命名化合物

PRODUCTS

生成物

结构：O=C(NCC(=O)N1CCN(CCN2CCCC2)CC1)c1ccc(S(=O)(=O)Nc2ccccc2C(=O)c2ccccc2)cc1

HCID24987825

未命名化合物

PROCEDURE

实验过程

The title compound was prepared from [4-(2-benzoyl-phenylsulfamoyl)-benzoylamino]-acetic acid and 1-(2-pyrrolidin-1-yl-ethyl)-piperazine (EMKA-Chemie) according to the method described in Example 1.1/f. MS (EI) 604.2 (MH+).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d8a796f53c144e4d9480d2b2b930d292
来源数据集: uspto-grants-2013_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08481527B2
来源说明: uspto-grants-2013_07

反应 SMILES

[C:1]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[NH:15][S:16]([C:19]1[CH:31]=[CH:30][C:22]([C:23]([NH:25][CH2:26][C:27]([OH:29])=O)=[O:24])=[CH:21][CH:20]=1)(=[O:18])=[O:17])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N:32]1([CH2:37][CH2:38][N:39]2[CH2:44][CH2:43][NH:42][CH2:41][CH2:40]2)[CH2:36][CH2:35][CH2:34][CH2:33]1>>[C:1]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[NH:15][S:16]([C:19]1[CH:31]=[CH:30][C:22]([C:23]([NH:25][CH2:26][C:27](=[O:29])[N:42]2[CH2:41][CH2:40][N:39]([CH2:38][CH2:37][N:32]3[CH2:33][CH2:34][CH2:35][CH2:36]3)[CH2:44][CH2:43]2)=[O:24])=[CH:21][CH:20]=1)(=[O:17])=[O:18])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1