HRID2190612

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID11464

4-Bromobenzoic acid

C7H5BrO2

结构：Cc1cc(N2CCNCC2)ccc1C(=O)Nc1cccc(C(C)(C)C)c1

HCID59318133

未命名化合物

结构：CC(C)(C)c1cccc(NC(=O)c2ccc(N3CCN(c4ccc(C(=O)O)cc4)CC3)c(F)c2)c1

HCID59318193

未命名化合物

PRODUCTS

生成物

结构：Cc1cc(N2CCN(c3ccc(C(=O)O)cc3)CC2)ccc1C(=O)Nc1cccc(C(C)(C)C)c1

HCID59318074

未命名化合物

PROCEDURE

实验过程

4-{4-[4-(3-tert-Butyl-phenylcarbamoyl)-3-methyl-phenyl]-piperazin-1-yl}-benzoic acid was synthesized by the coupling of N-(3-tert-butyl-phenyl)-2-methyl-4-piperazin-1-yl-benzamide and 4-bromo benzoic acid in a manner similar to the one described in the synthesis of 4-{4-[4-(3-tert-butyl-phenylcarbamoyl)-2-fluoro-phenyl]-piperazin-1-yl}-benzoic acid above. LCMS calcd for C29H33N3O3 (m/e) 471, obsd 472 (M+H).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-777a614a8d7a48d789b03024aa144028
来源数据集: uspto-grants-2012_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08324385B2
来源说明: uspto-grants-2012_12

反应 SMILES

[C:1]([C:5]1[CH:6]=[C:7]([NH:11][C:12](=[O:26])[C:13]2[CH:18]=[CH:17][C:16]([N:19]3[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]3)=[CH:15][C:14]=2[CH3:25])[CH:8]=[CH:9][CH:10]=1)([CH3:4])([CH3:3])[CH3:2].Br[C:28]1[CH:36]=[CH:35][C:31]([C:32]([OH:34])=[O:33])=[CH:30][CH:29]=1.C(C1C=C(NC(C2C=CC(N3CCN(C4C=CC(C(O)=O)=CC=4)CC3)=C(F)C=2)=O)C=CC=1)(C)(C)C>>[C:1]([C:5]1[CH:6]=[C:7]([NH:11][C:12]([C:13]2[CH:18]=[CH:17][C:16]([N:19]3[CH2:24][CH2:23][N:22]([C:28]4[CH:36]=[CH:35][C:31]([C:32]([OH:34])=[O:33])=[CH:30][CH:29]=4)[CH2:21][CH2:20]3)=[CH:15][C:14]=2[CH3:25])=[O:26])[CH:8]=[CH:9][CH:10]=1)([CH3:4])([CH3:3])[CH3:2]