HRID2178411

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID304978

2-(chloromethyl)-1,3-benzothiazole

C8H6ClNS

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

HCID90414810

未命名化合物

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

HCID90415263

未命名化合物

PRODUCTS

生成物

结构：CCOC(=O)C(C)(C)Cc1nc2cc(OCc3nc4ccccc4s3)ccc2n1Cc1ccc(Br)cc1

HCID90414595

未命名化合物

PROCEDURE

实验过程

The title compound was prepared using analogous conditions to those described for ethyl 3-(1-(4-bromobenzyl)-5-(quinolin-2-ylmethoxy)-1H-benzo[d]imidazol-2-yl)-2,2-dimethylpropanoate using ethyl 3-(1-(4-bromobenzyl)-5-hydroxy-1H-benzo[d]imidazol-2-yl)-2,2-dimethylpropanoate and 2-(chloromethyl)benzo[d]thiazole. MS (ESI): mass calcd. for C29H28BrN3O3S, 577.10; m/z found, 578.1 [M+H]+.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-fe78b7ef6fc243dbadb38780054c2896
来源数据集: uspto-grants-2015_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09067917B2
来源说明: uspto-grants-2015_06

反应 SMILES

[Br:1][C:2]1[CH:38]=[CH:37][C:5]([CH2:6][N:7]2[C:11]3[CH:12]=[CH:13][C:14]([O:16][CH2:17][C:18]4C=C[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]([CH3:36])([CH3:35])[C:30]([O:32][CH2:33][CH3:34])=[O:31])=[CH:4][CH:3]=1.BrC1C=CC(CN2C3C=CC(O)=CC=3N=C2CC(C)(C)C(OCC)=O)=CC=1.ClCC1[S:69]C2C=CC=CC=2N=1>>[S:69]1[C:25]2[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=2[N:19]=[C:18]1[CH2:17][O:16][C:14]1[CH:13]=[CH:12][C:11]2[N:7]([CH2:6][C:5]3[CH:37]=[CH:38][C:2]([Br:1])=[CH:3][CH:4]=3)[C:8]([CH2:28][C:29]([CH3:36])([CH3:35])[C:30]([O:32][CH2:33][CH3:34])=[O:31])=[N:9][C:10]=2[CH:15]=1