HRID1796179

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：O=C(O)C(COC1CCOCC1)CS(=O)(=O)Cc1ccccc1

HCID22053974

未命名化合物

HCID67301524

未命名化合物

PRODUCTS

生成物

结构：CC[C@H](NC(=O)C(COC1CCOCC1)CS(=O)(=O)Cc1ccccc1)C(=O)c1noc(-c2ccccc2)n1

HCID10007870

未命名化合物

PROCEDURE

实验过程

It is similarly prepared according to general procedure given for Example 1 above but using 2-Phenylmethanesulfonylmethyl-3-(tetrahydro-pyran-4-yloxy)-propionic acid and (S)-2-amino-1-(5-phenyl-1,2,4-oxadiazol-3-yl)-butan-1-ol.

WORKUP

后处理

customIt is similarly prepared

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-6f5a3d9c61534720ae990c50ee53f5c8
来源数据集: uspto-grants-2006_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07030116B2
来源说明: uspto-grants-2006_04

反应 SMILES

[C:1]1([CH2:7][S:8]([CH2:11][CH:12]([CH2:16][O:17][CH:18]2[CH2:23][CH2:22][O:21][CH2:20][CH2:19]2)[C:13]([OH:15])=O)(=[O:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:24][CH:25]([CH2:39][CH3:40])[C@@H:26]([C:28]1[N:32]=[C:31]([C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)[O:30][N:29]=1)[OH:27]>>[C:1]1([CH2:7][S:8]([CH2:11][CH:12]([CH2:16][O:17][CH:18]2[CH2:23][CH2:22][O:21][CH2:20][CH2:19]2)[C:13]([NH:24][C@H:25]([C:26]([C:28]2[N:32]=[C:31]([C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)[O:30][N:29]=2)=[O:27])[CH2:39][CH3:40])=[O:15])(=[O:9])=[O:10])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1