HRID2284307

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7579

4,4'-Diaminodiphenyl Ether

C12H12N2O

HCID18617591

4-(4-Hydroxy-1-piperidinyl)benzoic acid

C12H15NO3

PRODUCTS

生成物

结构：O=C(Nc1ccc(Oc2ccc(NC(=O)c3ccc(N4CCC(O)CC4)cc3)cc2)cc1)c1ccc(N2CCC(O)CC2)cc1

HCID67113510

未命名化合物

PROCEDURE

实验过程

Compound 914 was prepared according to the procedure described in Scheme IV from 4,4′-oxydianiline and 4-(4-hydroxypiperidin-1-yl)benzoic acid. [M+H]+ calcd for C36H38N4O5: 607.28; found 607.21.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-2e498f64b18e4a45b202e73b66b75a7d
来源数据集: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09144557B2
来源说明: uspto-grants-2015_09

反应 SMILES

[O:1]([C:9]1[CH:15]=[CH:14][C:12]([NH2:13])=[CH:11][CH:10]=1)[C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=1.[OH:16][CH:17]1[CH2:22][CH2:21][N:20]([C:23]2[CH:31]=[CH:30][C:26]([C:27](O)=[O:28])=[CH:25][CH:24]=2)[CH2:19][CH2:18]1>>[O:1]([C:9]1[CH:15]=[CH:14][C:12]([NH:13][C:27](=[O:28])[C:26]2[CH:30]=[CH:31][C:23]([N:20]3[CH2:21][CH2:22][CH:17]([OH:16])[CH2:18][CH2:19]3)=[CH:24][CH:25]=2)=[CH:11][CH:10]=1)[C:2]1[CH:3]=[CH:4][C:5]([NH:6][C:27](=[O:28])[C:26]2[CH:25]=[CH:24][C:23]([N:20]3[CH2:21][CH2:22][CH:17]([OH:16])[CH2:18][CH2:19]3)=[CH:31][CH:30]=2)=[CH:7][CH:8]=1