HRID1018615

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID573612

(1-Methyl-1H-imidazol-2-yl)methanol

C5H8N2O

结构：O=C(c1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCC2(CC1)C(=O)NC(=O)N2c1ccccc1Cl

HCID18401685

未命名化合物

PRODUCTS

生成物

结构：Cn1ccnc1CN1C(=O)N(c2ccccc2Cl)C2(CCN(C(=O)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)CC2)C1=O

HCID86584187

未命名化合物

PROCEDURE

实验过程

The title compound, MS: m/e=614.1 (M+H+), was prepared in accordance with the general method of example 121 from 8-(3,5-bis-trifluoromethyl-benzoyl)-1-(2-chloro-phenyl)-1,3,8-triaza-spiro[4.5]decane-2,4-dione and 1-methylimidazole-2-methanol.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-20cdbf803de1404ea0a8e468d53cf333
来源数据集: uspto-grants-2002_11
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06482829B2
来源说明: uspto-grants-2002_11

反应 SMILES

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