HRID2356960

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC1(C)CNc2cc(N3C(=O)N(Cc4ccncc4)C(C)(C)C3=O)ccc21

HCID66915685

未命名化合物

结构：CS(=O)(=O)OC1CN(C2CCCCC2)C1.O=C(O)C(=O)O

HCID86617226

未命名化合物

PRODUCTS

生成物

结构：CC1(C)CN(C2CN(C3CCCCC3)C2)c2cc(N3C(=O)N(Cc4ccncc4)C(C)(C)C3=O)ccc21

HCID66915698

未命名化合物

PROCEDURE

实验过程

prepared as described for example 96 by reaction of 3-(3,3-dimethyl-2,3-dihydro-1H-indol-6-yl)-5,5-dimethyl-1-pyridin-4-ylmethylimidazolidine-2,4-dione with 1-cyclohexylazetidin-3-yl methanesulphonate oxalate

WORKUP

后处理

customprepared

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-afe9de99249442478eff9833322ee466
来源数据集: uspto-grants-2010_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07759379B2
来源说明: uspto-grants-2010_07

反应 SMILES

[CH3:1][C:2]1([CH3:27])[C:10]2[C:5](=[CH:6][C:7]([N:11]3[C:15](=[O:16])[C:14]([CH3:18])([CH3:17])[N:13]([CH2:19][C:20]4[CH:25]=[CH:24][N:23]=[CH:22][CH:21]=4)[C:12]3=[O:26])=[CH:8][CH:9]=2)[NH:4][CH2:3]1.C(O)(=O)C(O)=O.CS(O[CH:39]1[CH2:42][N:41]([CH:43]2[CH2:48][CH2:47][CH2:46][CH2:45][CH2:44]2)[CH2:40]1)(=O)=O>>[CH:43]1([N:41]2[CH2:42][CH:39]([N:4]3[C:5]4[C:10](=[CH:9][CH:8]=[C:7]([N:11]5[C:15](=[O:16])[C:14]([CH3:17])([CH3:18])[N:13]([CH2:19][C:20]6[CH:25]=[CH:24][N:23]=[CH:22][CH:21]=6)[C:12]5=[O:26])[CH:6]=4)[C:2]([CH3:27])([CH3:1])[CH2:3]3)[CH2:40]2)[CH2:48][CH2:47][CH2:46][CH2:45][CH2:44]1