HRID1776706

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID4962834

未命名化合物

结构：CCOC(=O)C1(Cc2nc3cc(OCc4ccc5ccccc5n4)ccc3n2Cc2ccc(Br)cc2)CCCC1

HCID90414649

未命名化合物

PRODUCTS

生成物

结构：CCOC(=O)C(C)(Cc1nc2cc(OCc3ccc4ccccc4n3)ccc2n1Cc1ccc(Br)cc1)c1ccccc1

HCID90413918

未命名化合物

PROCEDURE

实验过程

The title compound was prepared using analogous conditions to those described for ethyl 1-((1-(4-bromobenzyl)-5-(quinolin-2-ylmethoxy)-1H-benzo[d]imidazol-2-yl)methyl)cyclopentanecarboxylate using racemic 3-methyl-3-phenyldihydrofuran-2,5-dione. MS (ESI): mass calcd. for C36H32BrN3O3, 633.16; m/z found, 634.1 [M+H]+.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-98580a80059d4510a10233b22fdbe8b3
来源数据集: uspto-grants-2016_02
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09265770B2
来源说明: uspto-grants-2016_02

反应 SMILES

[Br:1][C:2]1[CH:40]=[CH:39][C:5]([CH2:6][N:7]2[C:11]3[CH:12]=[CH:13][C:14]([O:16][CH2:17][C:18]4[CH:27]=[CH:26][C:25]5[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=5)[N:19]=4)=[CH:15][C:10]=3[N:9]=[C:8]2[CH2:28][C:29]2([C:34]([O:36][CH2:37][CH3:38])=[O:35])[CH2:33][CH2:32][CH2:31][CH2:30]2)=[CH:4][CH:3]=1.[CH3:41][C:42]1(C2C=CC=CC=2)CC(=O)O[C:43]1=O>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][N:7]2[C:11]3[CH:12]=[CH:13][C:14]([O:16][CH2:17][C:18]4[CH:27]=[CH:26][C:25]5[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=5)[N:19]=4)=[CH:15][C:10]=3[N:9]=[C:8]2[CH2:28][C:29]([CH3:30])([C:33]2[CH:32]=[CH:31][CH:43]=[CH:42][CH:41]=2)[C:34]([O:36][CH2:37][CH3:38])=[O:35])=[CH:39][CH:40]=1