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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Anhydride → 6-[(2-Oxopropyl)amino]pyridine-3-carboxylic acid

HRID 1838253
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인쇄 미리보기

반응식

HRID 1838253 반응식
[CH3:1][NH:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][N:4]=1.[C:12](OC(=O)C)(=[O:14])[CH3:13]>>[C:12]([CH2:1][NH:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][N:4]=1)(=[O:14])[CH3:13]
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참가 물질

3

반응물 2

HCID 7918Acetic AnhydrideHCID 222714156-(Methylamino)pyridine-3-carboxylic acid

생성물 1

HCID 187533126-[(2-Oxopropyl)amino]pyridine-3-carboxylic acid

실험 절차

A 1.5 g portion of 6-methylaminonicotinic acid in 20 ml of acetic anhydride was heated under reflux for 1.5 hours. After evaporation of the solvent under reduced pressure, the residue was dissolved with saturated aqueous sodium bicarbonate, and the aqueous layer was washed with ethyl acetate and then adjusted to pH 3 using concentrated hydrochloric acid. Then the aqueous layer was extracted with chloroform, the organic layer was washed and dried, and then the solvent was evaporated under reduced pressure to obtain 280 mg of the title compound as white crystals.

후처리

  1. temperatureunder reflux for 1.5 hours
  2. customAfter evaporation of the solvent under reduced pressure
  3. dissolutionthe residue was dissolved with saturated aqueous sodium bicarbonate
  4. washthe aqueous layer was washed with ethyl acetate
  5. extractionThen the aqueous layer was extracted with chloroform
  6. washthe organic layer was washed
  7. customdried
  8. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-959d8bb651d44dfabb5de79cbff7b980
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06673799B1

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