HRID2284184

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID69149

4,4'-Diaminobenzophenone

C13H12N2O

HCID86673982

未命名化合物

PRODUCTS

生成物

结构：O=C(Nc1ccc(C(=O)c2ccc(NC(=O)c3ccc(N4CCN(CCCO)CC4)cc3)cc2)cc1)c1ccc(N2CCN(CCCO)CC2)cc1

HCID67112620

未命名化合物

PROCEDURE

实验过程

Compound 318 was prepared according to the procedure described in Scheme IV from 4,4′-diaminobenzophenone and 4-(4-(3-hydroxypropyl)piperazino)benzoate. [M+H]+ calcd for C41H48N6O5: 705.37; found: 705.19.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d0f13b9658be4fc996a4dba4efc25350
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

[NH2:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([C:8]2[CH:13]=[CH:12][C:11]([NH2:14])=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1.[OH:17][CH2:18][CH2:19][CH2:20][N:21]1[CH2:26][CH2:25][N:24]([C:27]2[CH:35]=[CH:34][C:30]([C:31]([O-])=[O:32])=[CH:29][CH:28]=2)[CH2:23][CH2:22]1>>[C:6]([C:8]1[CH:13]=[CH:12][C:11]([NH:14][C:31](=[O:32])[C:30]2[CH:34]=[CH:35][C:27]([N:24]3[CH2:25][CH2:26][N:21]([CH2:20][CH2:19][CH2:18][OH:17])[CH2:22][CH2:23]3)=[CH:28][CH:29]=2)=[CH:10][CH:9]=1)([C:5]1[CH:15]=[CH:16][C:2]([NH:1][C:31](=[O:32])[C:30]2[CH:29]=[CH:28][C:27]([N:24]3[CH2:23][CH2:22][N:21]([CH2:20][CH2:19][CH2:18][OH:17])[CH2:26][CH2:25]3)=[CH:35][CH:34]=2)=[CH:3][CH:4]=1)=[O:7]