HRID1865402

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID84810

4-Morpholinecarbonyl chloride

C5H8ClNO2

结构：O=C(Nc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1cc(C=Cc2ccccc2)ccc1O

HCID72821885

未命名化合物

PRODUCTS

生成物

结构：O=C(Nc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1cc(C=Cc2ccccc2)ccc1OC(=O)N1CCOCC1

HCID85149143

未命名化合物

收率 99.5%

PROCEDURE

实验过程

Using 2-hydroxy-5-phenylethenyl-N-[3,5-bis(trifluoromethyl)-phenyl]benzamide and morpholine-4-carbonyl chloride as the raw materials, the same operation as the Example 71 gave the title compound.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-49355f5234644b11b152f000f0701979
来源数据集: uspto-grants-2009_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07626042B2
来源说明: uspto-grants-2009_12

反应 SMILES

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