HRID13336

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID23145109

未命名化合物

结构：CCOC(=O)c1ccccc1Oc1cc2nc(-c3ccccn3)[nH]c2cc1Oc1ccc(S(C)(=O)=O)cc1

HCID23145140

未命名化合物

PRODUCTS

生成物

结构：CS(=O)(=O)c1ccc(Oc2cc3[nH]c(-c4ccccn4)nc3cc2Oc2cccnc2OC(F)F)cc1

HCID23145275

未命名化合物

PROCEDURE

实验过程

The entitled compound was obtained as a pale yellow solid in the same method as in Example 14 or in accordance with the method or by combining it with an ordinary method but using 5-fluoro-4-(4-methanesulfonyl-phenoxy)-2-nitro-phenylamine obtained in Example 14 and 2-difluoromethoxy-pyridin-3-ol.

WORKUP

后处理

customThe entitled compound was obtained as a pale yellow solid in the same method as in Example 14 or in accordance with the method

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-12697cafd3ab4595aca6a3592bc87235
来源数据集: uspto-grants-2010_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07728025B2
来源说明: uspto-grants-2010_06

反应 SMILES

C(OC(C1C=[CH:37][CH:36]=[CH:35][C:7]=1[O:8][C:9]1[C:23]([O:24][C:25]2[CH:30]=[CH:29][C:28]([S:31]([CH3:34])(=[O:33])=[O:32])=[CH:27][CH:26]=2)=[CH:22][C:12]2[NH:13][C:14]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=3)=[N:15][C:11]=2[CH:10]=1)=O)C.[F:39][CH:40]([F:49])[O:41][C:42]1C(O)=CC=C[N:43]=1>>[F:39][CH:40]([F:49])[O:41][C:42]1[C:7]([O:8][C:9]2[C:23]([O:24][C:25]3[CH:26]=[CH:27][C:28]([S:31]([CH3:34])(=[O:32])=[O:33])=[CH:29][CH:30]=3)=[CH:22][C:12]3[NH:13][C:14]([C:16]4[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=4)=[N:15][C:11]=3[CH:10]=2)=[CH:35][CH:36]=[CH:37][N:43]=1