HRID735409

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：O=C(O)c1ccc(COc2ccc(-c3c4cccc(C(F)(F)F)c4nn3Cc3ccccc3)cc2)cc1

HCID11562429

未命名化合物

结构：COC(=O)c1ccc(Oc2ccc(-c3c4cccc(C(F)(F)F)c4nn3Cc3ccccc3)cc2)cc1

HCID67021156

未命名化合物

PRODUCTS

生成物

结构：O=C(O)c1ccc(Oc2ccc(-c3c4cccc(C(F)(F)F)c4nn3Cc3ccccc3)cc2)cc1

HCID11634528

未命名化合物

PROCEDURE

实验过程

This compound was prepared from 4-[4-(2-benzyl-7-trifluoromethyl-2H-indazol-3-yl)-phenoxy]-benzoic acid methyl ester in a way described for the preparation of 4-[4-(2-benzyl-7-trifluoromethyl-2H-indazol-3-yl)-phenoxymethyl]-benzoic acid (Example 2).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-015c18086b5d4a7391e84225ea846633
来源数据集: uspto-grants-2009_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07592363B2
来源说明: uspto-grants-2009_09

反应 SMILES

C[O:2][C:3](=[O:37])[C:4]1[CH:9]=[CH:8][C:7]([O:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[N:18]([CH2:30][C:31]4[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=4)[N:19]=[C:20]4[C:25]=3[CH:24]=[CH:23][CH:22]=[C:21]4[C:26]([F:29])([F:28])[F:27])=[CH:13][CH:12]=2)=[CH:6][CH:5]=1.C(N1C(C2C=CC(OCC3C=CC(C(O)=O)=CC=3)=CC=2)=C2C(C(C(F)(F)F)=CC=C2)=N1)C1C=CC=CC=1>>[CH2:30]([N:18]1[C:17]([C:14]2[CH:15]=[CH:16][C:11]([O:10][C:7]3[CH:8]=[CH:9][C:4]([C:3]([OH:37])=[O:2])=[CH:5][CH:6]=3)=[CH:12][CH:13]=2)=[C:25]2[C:20]([C:21]([C:26]([F:29])([F:27])[F:28])=[CH:22][CH:23]=[CH:24]2)=[N:19]1)[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1