HRID27941

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID21163943

未命名化合物

HCID54204673

未命名化合物

HCID86737228

未命名化合物

PRODUCTS

生成物

结构：CC(C)C(C(=O)OC(C#N)c1cccc(Oc2ccccc2F)n1)c1cc2cc(Cl)ccc2s1

HCID53698829

未命名化合物

HCID86737227

未命名化合物

PROCEDURE

实验过程

The alcohol, cyano [6-(3,4-dimethoxyphenyl)-2-pyridyl] methanol and cyano [6-(2-fluorophenoxy)-2-pyridyl]methanol, is reacted with the acid chloride of 2-(5-chloro-2-benzothienyl)-3-methylbutanoic acid to yield cyano[6-(3,4-dimethoxy-phenoxy)-2-pyridyl]methyl 2-(5-chloro-2-benzothienyl-3-methylbutanoate and cyano[6-(2-fluorophenoxy)-2-pyridyl]methyl 2-(5-chloro-2-benzothienyl)-3-methylbutanoate.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-b7f9ee29f1a54a7b8ec9bfa71b21d33a
来源数据集: uspto-grants-1980_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04224330
来源说明: uspto-grants-1980_09

反应 SMILES

C(C(C1C=CC=C(C2C=CC(OC)=C(OC)C=2)N=1)O)#N.[C:21]([CH:23]([C:25]1[CH:30]=[CH:29][CH:28]=[C:27]([O:31][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][C:33]=2[F:38])[N:26]=1)[OH:24])#[N:22].[Cl:39][C:40]1[CH:41]=[CH:42][C:43]2[S:47][C:46]([CH:48]([CH:52]([CH3:54])[CH3:53])[C:49]([OH:51])=[O:50])=[CH:45][C:44]=2[CH:55]=1>>[Cl:39][C:40]1[CH:41]=[CH:42][C:43]2[S:47][C:46]([CH:48]([CH:52]([CH3:53])[CH3:54])[C:49]([O-:51])=[O:50])=[CH:45][C:44]=2[CH:55]=1.[Cl:39][C:40]1[CH:41]=[CH:42][C:43]2[S:47][C:46]([CH:48]([CH:52]([CH3:53])[CH3:54])[C:49]([O:24][CH:23]([C:21]#[N:22])[C:25]3[CH:30]=[CH:29][CH:28]=[C:27]([O:31][C:32]4[CH:37]=[CH:36][CH:35]=[CH:34][C:33]=4[F:38])[N:26]=3)=[O:50])=[CH:45][C:44]=2[CH:55]=1