HRID1662635

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：COc1ccccc1C1(CC(=O)N2CCN(c3cccnn3)CC2)C(=O)Nc2ccc(Cl)cc21

HCID67429841

未命名化合物

HCID86625684

未命名化合物

PRODUCTS

生成物

结构：COc1ccc(S(=O)(=O)N2C(=O)C(CC(=O)N3CCN(c4cccnn4)CC3)(c3ccccc3OC)c3cc(Cl)ccc32)c(OC(F)(F)F)c1

HCID11951091

未命名化合物

收率 75.3%

PROCEDURE

实验过程

With 170 mg of the compound obtained in Step 49-1 and 114 mg of 4-methoxy-2-(trifluoromethoxy)benzene sulfonyl chloride as starting materials, 196 mg of the title compound (colorless amorphous) was obtained by a similar method to Example 2.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-5035c5cd57b1448da6c4c16c417be831
来源数据集: uspto-grants-2011_10
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08030499B2
来源说明: uspto-grants-2011_10

反应 SMILES

[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[C:5]2([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1[O:33][CH3:34])[CH2:12][C:13](=[O:26])[N:14]1[CH2:19][CH2:18][N:17]([C:20]2[N:21]=[N:22][CH:23]=[CH:24][CH:25]=2)[CH2:16][CH2:15]1.[CH3:35][O:36][C:37]1[CH:42]=[CH:41][C:40]([S:43](Cl)(=[O:45])=[O:44])=[C:39]([O:47][C:48]([F:51])([F:50])[F:49])[CH:38]=1>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([S:43]([C:40]1[CH:41]=[CH:42][C:37]([O:36][CH3:35])=[CH:38][C:39]=1[O:47][C:48]([F:49])([F:50])[F:51])(=[O:45])=[O:44])[C:6](=[O:11])[C:5]2([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1[O:33][CH3:34])[CH2:12][C:13](=[O:26])[N:14]1[CH2:15][CH2:16][N:17]([C:20]2[N:21]=[N:22][CH:23]=[CH:24][CH:25]=2)[CH2:18][CH2:19]1