HRID736929

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：Nc1c(Cl)cc(CC(CC(=O)N2CCC(N3Cc4ccccc4NC3=O)CC2)C(=O)O)cc1C(F)(F)F

HCID12094449

未命名化合物

HCID57848475

未命名化合物

PRODUCTS

生成物

结构：Nc1c(Cl)cc(CC(CC(=O)N2CCC(N3Cc4ccccc4NC3=O)CC2)C(=O)N2CCC(N3CCN(CC(=O)O)CC3)CC2)cc1C(F)(F)F

HCID10462774

未命名化合物

PROCEDURE

实验过程

Prepared analogously to Example 16.4 from 108 mg (0.20 mmol) 2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-4-oxo-4-[4-(2-oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidin-1-yl]-butanoic acid and 51 mg (0.20 mmol) ethyl(4-piperidin-4-yl-piperazin-1-yl)-acetate.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-c4c3572c3cc840f38097f052a7450f1e
来源数据集: uspto-grants-2009_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07595312B2
来源说明: uspto-grants-2009_09

反应 SMILES

[NH2:1][C:2]1[C:32]([C:33]([F:36])([F:35])[F:34])=[CH:31][C:5]([CH2:6][CH:7]([CH2:11][C:12](=[O:30])[N:13]2[CH2:18][CH2:17][CH:16]([N:19]3[CH2:28][C:27]4[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=4)[NH:21][C:20]3=[O:29])[CH2:15][CH2:14]2)[C:8](O)=[O:9])=[CH:4][C:3]=1[Cl:37].C([O:40][C:41](=[O:55])[CH2:42][N:43]1[CH2:48][CH2:47][N:46]([CH:49]2[CH2:54][CH2:53][NH:52][CH2:51][CH2:50]2)[CH2:45][CH2:44]1)C>>[NH2:1][C:2]1[C:32]([C:33]([F:35])([F:34])[F:36])=[CH:31][C:5]([CH2:6][CH:7]([CH2:11][C:12](=[O:30])[N:13]2[CH2:18][CH2:17][CH:16]([N:19]3[CH2:28][C:27]4[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=4)[NH:21][C:20]3=[O:29])[CH2:15][CH2:14]2)[C:8]([N:52]2[CH2:51][CH2:50][CH:49]([N:46]3[CH2:45][CH2:44][N:43]([CH2:42][C:41]([OH:40])=[O:55])[CH2:48][CH2:47]3)[CH2:54][CH2:53]2)=[O:9])=[CH:4][C:3]=1[Cl:37]