HRID1875756

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：COC(=O)C1CCC(COS(=O)(=O)c2ccc(C)cc2)CC1

HCID59460667

未命名化合物

结构：Oc1cc(Cl)ccc1-c1nc2cc(F)c(F)cc2n1CC1CCCCC1

HCID136378478

未命名化合物

PRODUCTS

生成物

结构：COC(=O)C1CCC(COc2cc(Cl)ccc2-c2nc3cc(F)c(F)cc3n2CC2CCCCC2)CC1

HCID67049710

未命名化合物

PROCEDURE

实验过程

The title compound was prepared in analogy to Example 5, intermediate a, from 5-chloro-2-(1-cyclohexylmethyl-5,6-difluoro-1H-benzoimidazol-2-yl)-phenol (Example 19, intermediate a) and 4-(toluene-4-sulfonyloxymethyl)-cyclohexane carboxylic acid methyl ester (CAS Reg. No. 1003013-11-3). Brown solid (51%). MS (Turbo Spray): m/z=531.4 (M+H).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-fa0a505047e2483fad8d1b45400d17ad
来源数据集: uspto-grants-2012_11
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08309581B2
来源说明: uspto-grants-2012_11

反应 SMILES

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