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Potassium Carbonate → HCID 14720280、化合物

HRID 2351964
ノート
印刷プレビュー

反応式

HRID 2351964 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][CH2:9][C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH3:22][N:23]([CH3:28])[S:24](Cl)(=[O:26])=[O:25]>ClCCl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]([CH2:9][C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[S:24]([N:23]([CH3:28])[CH3:22])(=[O:26])=[O:25])=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 83372Dimethylsulphamoyl chlorideHCID 28045454-chloro-N-(pyridin-3-ylmethyl)aniline

生成物 1

HCID 14720280HCID 14720280、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A 2.8 g. portion of 3-(4-chlorophenylaminomethyl)pyridine was dissolved in dichloromethane, and to it was added 2.1 g. of potassium carbonate and 1.6 ml. of dimethylsulfamoyl chloride. The mixture was stirred at ambient temperature for 1 day, and was then stirred under gentle heating for 3 days. The solvent was then evaporated under vacuum, and the oily residue was purified by chromatography on silica gel in chloroform to obtain 3.9 g. of the desired product. Its elemental analysis was as follows.

後処理

  1. additionto it was added 2.1 g
  2. stirringwas then stirred
  3. temperatureunder gentle heating for 3 days
  4. customThe solvent was then evaporated under vacuum
  5. customthe oily residue was purified by chromatography on silica gel in chloroform
  6. customto obtain 3.9 g

出典と根拠

ORDレコード
ord-c649b2aa0cff468ea4a3ff93e1391b12
出典データセット
uspto-grants-1989_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04874775

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート