HRID32085

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：O=C(O)CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1

HCID3632641

未命名化合物

HCID58841352

未命名化合物

PRODUCTS

生成物

结构：COC(=O)c1ccc2c(c1)N(C)S(=O)(=O)CC2NC(=O)CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1

HCID68932321

未命名化合物

PROCEDURE

实验过程

The title compound was prepared from 3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionic acid Example 1, Step H and 4-amino-1-methyl-2,2-dioxo-1,2,3,4-tetrahydro-2λ6-benzo[c][1,2]thiazine-7-carboxylic acid methyl ester (Step B) similar to that described in Example 1, Step F. MS (+APCI, m/z): 608 (M+H)+.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-bf81950fa04d4f2088e42476cf0f6e96
来源数据集: uspto-grants-2008_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07425631B2
来源说明: uspto-grants-2008_09

反应 SMILES

[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[S:11]([NH:14][CH:15]([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH2:16][C:17](O)=[O:18])(=[O:13])=[O:12].[CH3:26][O:27][C:28]([C:30]1[CH:31]=[CH:32][C:33]2[CH:38]([NH2:39])[CH2:37][S:36](=[O:41])(=[O:40])[N:35]([CH3:42])[C:34]=2[CH:43]=1)=[O:29]>>[CH3:26][O:27][C:28]([C:30]1[CH:31]=[CH:32][C:33]2[CH:38]([NH:39][C:17](=[O:18])[CH2:16][CH:15]([NH:14][S:11]([C:2]3[CH:3]=[CH:4][C:5]4[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=4)[CH:1]=3)(=[O:13])=[O:12])[C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:37][S:36](=[O:41])(=[O:40])[N:35]([CH3:42])[C:34]=2[CH:43]=1)=[O:29]