HRID1366854

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID204419

Benzenesulfonyl chloride, 2,4-dichloro-

C6H3Cl3O2S

结构：CCCCCOC(=O)c1cc(N)ncc1Sc1ccc(S(=O)(=O)N2CCCCC2)cc1

HCID57718213

未命名化合物

PRODUCTS

生成物

结构：CCCCCOC(=O)c1cc(NS(=O)(=O)c2ccc(Cl)cc2Cl)ncc1Sc1ccc(S(=O)(=O)N2CCCCC2)cc1

HCID57718221

未命名化合物

收率 29,327.1%

AUXILIARIES

试剂、催化剂与溶剂

催化剂HCID14284

N,N-Dimethylpyridin-4-amine

C7H10N2

溶剂HCID1049

Pyridine

C5H5N

PROCEDURE

实验过程

A solution of the 2-amino-5-[4-(piperidine-1-sulfonyl) -phenylsulfanyl]-isonicotinic acid pentyl ester (500 mg, 1.1 μmol), 2,4-dichlorobenzenesulfonylchloride (327 mg, 1.33 mmol) and 4-dimethylaminopyridine (134 mg, 1.1 mmol) in pyridine (10 ml) was stirred at 40° C. overnight. The pyridine was removed under reduced pressure and the residue purified by flash column chromatography using ethyl acetate 1/2 hexane as eluent to afford 2-(2,4-dichloro-benzenesulfonylamino)-5-[4-(piperidine-1-sulfonyl)-phenylsulfanyl]-isonicotinic acid pentyl ester as a yellow foam (217 mg, 29%).

WORKUP

后处理

customThe pyridine was removed under reduced pressure
customthe residue purified by flash column chromatography

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-84c80da2f5d24931afae529d62f091ea
来源数据集: uspto-grants-2011_02
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07893077B2
来源说明: uspto-grants-2011_02

反应 SMILES

[CH2:1]([O:6][C:7](=[O:31])[C:8]1[C:13]([S:14][C:15]2[CH:20]=[CH:19][C:18]([S:21]([N:24]3[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]3)(=[O:23])=[O:22])=[CH:17][CH:16]=2)=[CH:12][N:11]=[C:10]([NH2:30])[CH:9]=1)[CH2:2][CH2:3][CH2:4][CH3:5].[Cl:32][C:33]1[CH:38]=[C:37]([Cl:39])[CH:36]=[CH:35][C:34]=1[S:40](Cl)(=[O:42])=[O:41]>CN(C)C1C=CN=CC=1.N1C=CC=CC=1>[CH2:1]([O:6][C:7](=[O:31])[C:8]1[C:13]([S:14][C:15]2[CH:16]=[CH:17][C:18]([S:21]([N:24]3[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]3)(=[O:23])=[O:22])=[CH:19][CH:20]=2)=[CH:12][N:11]=[C:10]([NH:30][S:40]([C:34]2[CH:35]=[CH:36][C:37]([Cl:39])=[CH:38][C:33]=2[Cl:32])(=[O:42])=[O:41])[CH:9]=1)[CH2:2][CH2:3][CH2:4][CH3:5]