HRID1782771

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID20132751

Methyl azetidine-3-carboxylate

C5H9NO2

结构：CCOC(=O)c1ccc(OCCCc2ccc(OCCCCOc3ccccc3)cc2)c(C(=O)O)c1

HCID57589233

未命名化合物

PRODUCTS

生成物

结构：CCOC(=O)c1ccc(OCCCc2ccc(OCCCCOc3ccccc3)cc2)c(C(=O)N2CC(C(=O)OC)C2)c1

HCID57589054

未命名化合物

PROCEDURE

实验过程

The compound is prepared in analogy to the process described in Example 6 from 5-(ethoxycarbonyl)-2-{3-[4-(4-phenoxybutoxy)phenyl]propoxy}benzoic acid and methyl 3-azetidinecarboxylate [CAS No. 343238-58-4]. The crude product is immediately reacted further without purification.

WORKUP

后处理

customThe compound is prepared in analogy to the process

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-7466348edf73467aa2ea84e6b996d0dc
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

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