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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetyl chloride → HCID 68955615, 화합물

HRID 1455635
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인쇄 미리보기

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HRID 1455635 반응식
[Br:1][C:2]1[CH:3]=[C:4]([C:8](=[N:10][OH:11])[NH2:9])[CH:5]=[N:6][CH:7]=1.[C:12](Cl)(=O)[CH3:13]>N1C=CC=CC=1.CCOC(C)=O.C([O-])(O)=O.[Na+]>[Br:1][C:2]1[CH:7]=[N:6][CH:5]=[C:4]([C:8]2[N:9]=[C:12]([CH3:13])[O:11][N:10]=2)[CH:3]=1
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참가 물질

6

반응물 2

HCID 6367Acetyl chloride2회HCID 737396465-bromo-N-hydroxynicotinamidine

생성물 1

HCID 68955615HCID 68955615, 화합물

시약·촉매·용매 3

HCID 1049Pyridine용매HCID 8857Ethyl Acetate용매HCID 516892Sodium Bicarbonate용매

반응 조건

온도
100 °C

실험 절차

To a solution of 5-bromo-N′-hydroxypyridine-3-carboximidamide (1.0 eq.) in pyridine was added acetyl chloride (2 eq). The reaction stirred at 100° C. for 1 h and 2 eq of acetyl chloride was added. After 1 h, the mixture was cooled, diluted with EtOAc and aqueous NaHCO3. The organic extracts were washed with aqueous NaHCO3, brine, dried over Na2SO4, filtered and concentrated. Flash chromatography (Hex:EtOAc; 70:30) afforded the title compound as a white solid.

후처리

  1. waitAfter 1 h
  2. temperaturethe mixture was cooled
  3. washThe organic extracts were washed with aqueous NaHCO3, brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-34748353cc7147f18bf80fe0931b3dd7
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07482456B2

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