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Potassium Carbonate → HCID 14720280, 화합물

HRID 2351964
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HRID 2351964 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

HCID 14720280HCID 14720280, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-c649b2aa0cff468ea4a3ff93e1391b12
출처 데이터셋
uspto-grants-1989_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04874775

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