HRID1161343

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：O=C(O)C(C1CCCCC1)n1c(-c2ccc(Cl)cc2)nc2cc(F)c(F)cc21

HCID66619321

未命名化合物

HCID67131121

未命名化合物

结构：CCOC(=O)c1ccc(NC(=O)C(C2CCCCC2)n2c(-c3ccc(Cl)cc3)nc3cc(F)c(F)cc32)cc1

HCID68645493

未命名化合物

PRODUCTS

生成物

结构：COC(=O)C1(Oc2ccc(NC(=O)C(C3CCCCC3)n3c(-c4ccc(Cl)cc4)nc4cc(F)c(F)cc43)c(F)c2)CC1

HCID68645482

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

催化剂HCID14284

N,N-Dimethylpyridin-4-amine

C7H10N2

PROCEDURE

实验过程

This compound was prepared in analogy to example 22, intermediate d, from [2-(4-chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-cyclohexyl-acetic acid, 1-(4-amino-3-fluoro-phenoxy)-cyclopropanecarboxylic acid methyl ester and using 4-(dimethylamino)pyridine as base.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-08d042bac46b43e1a66ae155655a6315
来源数据集: uspto-grants-2010_10
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07816540B2
来源说明: uspto-grants-2010_10

反应 SMILES

C(OC(=O)C1C=CC(N[C:12](=[O:38])[CH:13]([N:20]2[C:24]3[CH:25]=[C:26]([F:30])[C:27]([F:29])=[CH:28][C:23]=3[N:22]=[C:21]2[C:31]2[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][CH:32]=2)[CH:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)=CC=1)C.ClC1C=CC(C2N(C(C3CCCCC3)C(O)=O)C3C=C(F)C(F)=CC=3N=2)=CC=1.[CH3:68][O:69][C:70]([C:72]1([O:75][C:76]2[CH:81]=[CH:80][C:79]([NH2:82])=[C:78]([F:83])[CH:77]=2)[CH2:74][CH2:73]1)=[O:71]>CN(C)C1C=CN=CC=1>[CH3:68][O:69][C:70]([C:72]1([O:75][C:76]2[CH:81]=[CH:80][C:79]([NH:82][C:12](=[O:38])[CH:13]([N:20]3[C:24]4[CH:25]=[C:26]([F:30])[C:27]([F:29])=[CH:28][C:23]=4[N:22]=[C:21]3[C:31]3[CH:32]=[CH:33][C:34]([Cl:37])=[CH:35][CH:36]=3)[CH:14]3[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19]3)=[C:78]([F:83])[CH:77]=2)[CH2:74][CH2:73]1)=[O:71]