HRID1782768

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID57443753

未命名化合物

结构：COC(=O)c1ccc(O)c(C(=O)N2CCC(C(=O)OC)CC2)c1

HCID57589141

未命名化合物

PRODUCTS

生成物

结构：COC(=O)c1ccc(OCCCc2ccc(OCCCCOc3ccccc3)cc2)c(C(=O)N2CCC(C(=O)OC)CC2)c1

HCID57589081

未命名化合物

PROCEDURE

实验过程

Methyl 1-(5-(methoxycarbonyl)-2-{3-[4-(4-phenoxybutoxy)phenyl]propoxy}-benzoyl)-4-piperidinecarboxylate is prepared in analogy to the process described in Example 2 from 1-(3-bromopropyl)-4-(4-phenoxybutoxy)benzene and methyl 1-[2-hydroxy-5-(methoxycarbonyl)benzoyl]-4-piperidinecarboxylate.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-b84c59f2dcf04e7f80bc6f293a54a439
来源数据集: uspto-grants-2009_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07498460B2
来源说明: uspto-grants-2009_03

反应 SMILES

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