HRID1659611

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1c1ccccc1C(F)(F)F

HCID168089

SK&F 24260

C20H22F3NO4

HCID131712575

未命名化合物

PRODUCTS

生成物

结构：CCOC(=O)C1=C(C)Nc2cc(-c3ccccc3)n(-c3ccccn3)c(=O)c2C1c1ccccc1C(F)(F)F

HCID20559742

未命名化合物

PROCEDURE

实验过程

This product is obtained using the procedure of Example 1, from diethyl 1,4-dihydro-4-(2-trifluoromethylphenyl)2,6-dimethyl-3,5-pyridine dicarboxylate and N-(2-pyridyl)-benzimidoyl chloride HCl (2.5 g, 9.4%).

WORKUP

后处理

customThis product is obtained

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-6d67859092554e968e6a7211adb870b3
来源数据集: uspto-grants-1981_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04304914
来源说明: uspto-grants-1981_12

反应 SMILES

[F:1][C:2]([F:28])([F:27])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH:9]1[C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[C:13]([CH3:20])[NH:12][C:11]([CH3:21])=[C:10]1[C:22]([O:24]CC)=O.Cl.[N:30]1[CH:35]=[CH:34][CH:33]=[CH:32][C:31]=1[N:36]=[C:37](Cl)[C:38]1[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1>>[CH3:20][C:13]1[NH:12][C:11]2[CH:21]=[C:37]([C:38]3[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=3)[N:36]([C:31]3[CH:32]=[CH:33][CH:34]=[CH:35][N:30]=3)[C:22](=[O:24])[C:10]=2[CH:9]([C:4]2[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=2[C:2]([F:28])([F:1])[F:27])[C:14]=1[C:15]([O:17][CH2:18][CH3:19])=[O:16]