HRID1413098

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID12850226

未命名化合物

HCID20293459

未命名化合物

HCID53885514

未命名化合物

PRODUCTS

生成物

结构：CC(OC(=O)C(C=Cc1ccc(F)cc1)C(C)C)c1cccc(Oc2ccccc2)n1

HCID54189122

未命名化合物

结构：CC(OC(=O)C(C=Cc1ccc(F)cc1)C(C)C)c1cccc(Oc2ccc(F)cc2)n1

HCID54316819

未命名化合物

PROCEDURE

实验过程

Following the procedure of Example 3, each of methyl(6-phenoxy-2-pyridyl)methanol and methyl[6-(4-fluorophenoxy)-2-pyridyl]methanol is reacted with 4-(4-fluorophenyl)-2-isopropyl-3-butenoic acid to yield methyl(6-phenoxy-2-pyridyl)methyl 4-(4-fluorophenyl)-2-isopropyl-3-butenoate and methyl[6-(4-fluorophenoxy)-2-pyridyl]methyl 4-(4-fluorophenyl)-2-isopropyl-3-butenoate, respectively.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-1085acdaf7d7427c8eed35abbf73a2e1
来源数据集: uspto-grants-1981_02
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04248875
来源说明: uspto-grants-1981_02

反应 SMILES

[CH3:1][CH:2]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([O:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[N:5]=1)[OH:3].[CH3:17][CH:18]([C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([O:26][C:27]2[CH:32]=[CH:31][C:30]([F:33])=[CH:29][CH:28]=2)[N:21]=1)[OH:19].[F:34][C:35]1[CH:40]=[CH:39][C:38]([CH:41]=[CH:42][CH:43]([CH:47]([CH3:49])[CH3:48])[C:44](O)=[O:45])=[CH:37][CH:36]=1>>[F:34][C:35]1[CH:36]=[CH:37][C:38]([CH:41]=[CH:42][CH:43]([CH:47]([CH3:49])[CH3:48])[C:44]([O:3][CH:2]([CH3:1])[C:4]2[CH:9]=[CH:8][CH:7]=[C:6]([O:10][C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[N:5]=2)=[O:45])=[CH:39][CH:40]=1.[F:34][C:35]1[CH:36]=[CH:37][C:38]([CH:41]=[CH:42][CH:43]([CH:47]([CH3:49])[CH3:48])[C:44]([O:19][CH:18]([CH3:17])[C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([O:26][C:27]3[CH:32]=[CH:31][C:30]([F:33])=[CH:29][CH:28]=3)[N:21]=2)=[O:45])=[CH:39][CH:40]=1