HRID50424

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID66054

Butanoyl chloride, 3-methyl-

C5H9ClO

结构：CCc1nc2c(C)cc(C)nc2n1-c1ccc(CCNC(=O)NS(=O)(=O)c2ccc(C)cc2)cc1

HCID9935367

未命名化合物

PRODUCTS

生成物

结构：Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(CC(C)C)nc4c(C)cc(C)nc43)cc2)cc1

HCID21876014

未命名化合物

PROCEDURE

实验过程

The title compound was prepared according to the procedure described in step 5 of Example 1 from 2-{4-[(3-amino-4,6-dimethyl-2-pyridinyl)amino]phenyl}ethanol (step 4 of Example 1) and isovaleryl chloride.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-72811ec940cb42a5ab6b4ba19f5ba60a
来源数据集: uspto-grants-2004_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06710054B2
来源说明: uspto-grants-2004_03

反应 SMILES

C(C1[N:13]([C:14]2[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][NH:22][C:23]([NH:25][S:26]([C:29]3[CH:34]=[CH:33][C:32]([CH3:35])=[CH:31][CH:30]=3)(=[O:28])=[O:27])=[O:24])=[CH:16][CH:15]=2)[C:6]2=[N:7][C:8]([CH3:12])=[CH:9][C:10]([CH3:11])=[C:5]2[N:4]=1)C.[C:36](Cl)(=O)[CH2:37][CH:38]([CH3:40])[CH3:39]>>[CH2:37]([C:36]1[N:13]([C:14]2[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][NH:22][C:23]([NH:25][S:26]([C:29]3[CH:30]=[CH:31][C:32]([CH3:35])=[CH:33][CH:34]=3)(=[O:28])=[O:27])=[O:24])=[CH:16][CH:15]=2)[C:6]2=[N:7][C:8]([CH3:12])=[CH:9][C:10]([CH3:11])=[C:5]2[N:4]=1)[CH:38]([CH3:40])[CH3:39]