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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetyl chloride → N-(5,6-dichloro-3-nitropyrazin-2-yl)acetamide

HRID 1648849
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HRID 1648849 반응식
[Cl:1][C:2]1[N:3]=[C:4]([N+:10]([O-:12])=[O:11])[C:5]([NH2:9])=[N:6][C:7]=1[Cl:8].C(=O)(O)[O-].[Na+].[C:18](Cl)(=[O:20])[CH3:19]>>[Cl:1][C:2]1[N:3]=[C:4]([N+:10]([O-:12])=[O:11])[C:5]([NH:9][C:18](=[O:20])[CH3:19])=[N:6][C:7]=1[Cl:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6367Acetyl chlorideHCID 516892Sodium BicarbonateHCID 130629765,6-Dichloro-3-nitropyrazin-2-amine

생성물 1

HCID 13062977N-(5,6-dichloro-3-nitropyrazin-2-yl)acetamide

실험 절차

To 1.0 g of 5,6-dichloro-3-nitropyrazinamine in 15 ml acetyl chloride under nitrogen atmosphere at room temperature is added 0.84 g anhydrous sodium bicarbonate. The reaction mixture is then stirred and heated at reflux for 4 days. Excess acetyl chloride is then removed in vacuo and the residue is chromatographed on silica gel. The desired product is eluted from the column with chloroform.

후처리

  1. temperatureheated
  2. temperatureat reflux for 4 days
  3. customExcess acetyl chloride is then removed in vacuo
  4. customthe residue is chromatographed on silica gel
  5. washThe desired product is eluted from the column with chloroform

출처 및 근거

ORD 기록
ord-d6a57bb30bf646fd85f8e6fb45d7d8f0
출처 데이터셋
uspto-grants-1983_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04414215

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