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Potassium Carbonate → HCID 14720310、化合物

HRID 2351982
ノート
印刷プレビュー

反応式

HRID 2351982 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][CH2:9][C:10]2[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=2)=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH3:22][S:23](Cl)(=[O:25])=[O:24]>ClCCl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]([CH2:9][C:10]2[CH:11]=[CH:12][N:13]=[CH:14][CH:15]=2)[S:23]([CH3:22])(=[O:25])=[O:24])=[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 31297Methanesulfonyl chloride2 回HCID 9643524-chloro-N-(pyridin-4-ylmethyl)aniline

生成物 1

HCID 14720310HCID 14720310、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A 3.3 g. portion of 4-(4-chlorophenylaminomethyl)pyridine was dissolved in 15 ml. of dichloromethane, and 2.7 g. of potassium carbonate and 1.6 ml. of methanesulfonyl chloride were added. The mixture was stirred at ambient temperature for several days, adding another 0.5 ml. of methanesulfonyl chloride in the process. The mixture was then diluted with dichloromethane, extracted with aqueous sodium bicarbonate and with water, dried over magnesium sulfate and evaporated. The residue was taken up in dichloromethane and chromatographed over silica gel, eluting first with dichloromethane and then with 9:1 dichloromethane:ethyl acetate. The product-containing fractions were combined and evaporated, and the residue was triturated with petroleum ether and diethyl ether to obtain 2.1 g. of the desired product.

後処理

  1. additionadding another 0.5 ml
  2. extractionextracted with aqueous sodium bicarbonate and with water
  3. dry with materialdried over magnesium sulfate
  4. customevaporated
  5. customchromatographed over silica gel
  6. washeluting first with dichloromethane
  7. customevaporated
  8. customthe residue was triturated with petroleum ether and diethyl ether
  9. customto obtain 2.1 g

出典と根拠

ORDレコード
ord-420ce333902c4b84bd59d6da2ed2a76f
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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