HRID2121993

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CSc1sc2c([n+]1C)CCCC2.Cc1ccc(S(=O)(=O)[O-])cc1

HCID21937526

未命名化合物

结构：CCNc1ccc(C(C)=O)cc1N=C1SCC(=O)N1Cc1ccccc1

HCID21937583

未命名化合物

PRODUCTS

生成物

结构：CCNc1ccc(C(C)=O)cc1N=C1SC(=C2SC3=C(CCCC3)N2C)C(=O)N1Cc1ccccc1

HCID72639863

未命名化合物

PROCEDURE

实验过程

The title compound was prepared in a manner similar to Example 168 by condensing intermediate 3-methyl-2-methylthio-4,5,6,7-tetrahydrobenzothiazol-3-ium p-toluenesulfonate with 2-(5-acetyl-2-ethylaminophenylimino)-3-benzylthiazolidin-4-one. MS(ESI): 519 (MH+).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-b22199f9a01e4e96b47bf351c2950d5f
来源数据集: uspto-grants-2004_02
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06696473B2
来源说明: uspto-grants-2004_02

反应 SMILES

C1(C)C=CC(S([O-])(=O)=O)=CC=1.[CH3:12][N+:13]1[C:17]2[CH2:18][CH2:19][CH2:20][CH2:21][C:16]=2[S:15][C:14]=1SC.[C:24]([C:27]1[CH:28]=[CH:29][C:30]([NH:47][CH2:48][CH3:49])=[C:31]([N:33]=[C:34]2[N:38]([CH2:39][C:40]3[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=3)[C:37](=[O:46])[CH2:36][S:35]2)[CH:32]=1)(=[O:26])[CH3:25]>>[C:24]([C:27]1[CH:28]=[CH:29][C:30]([NH:47][CH2:48][CH3:49])=[C:31]([N:33]=[C:34]2[N:38]([CH2:39][C:40]3[CH:41]=[CH:42][CH:43]=[CH:44][CH:45]=3)[C:37](=[O:46])[C:36](=[C:14]3[N:13]([CH3:12])[C:17]4[CH2:18][CH2:19][CH2:20][CH2:21][C:16]=4[S:15]3)[S:35]2)[CH:32]=1)(=[O:26])[CH3:25]