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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N-(3-Formyl-2-pyridinyl)-2,2-dimethylpropanamide → 3-Pyridinecarboxaldehyde, 2-amino-

HRID 229030
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HRID 229030 반응식
[CH:1]([C:3]1[C:4]([NH:9]C(=O)C(C)(C)C)=[N:5][CH:6]=[CH:7][CH:8]=1)=[O:2]>Cl>[NH2:9][C:4]1[C:3]([CH:1]=[O:2])=[CH:8][CH:7]=[CH:6][N:5]=1
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참가 물질

3

반응물 1

HCID 736837N-(3-Formyl-2-pyridinyl)-2,2-dimethylpropanamide

생성물 1

HCID 7376333-Pyridinecarboxaldehyde, 2-amino-수율 88%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

N-(3-Formyl-pyridin-2-yl)-2,2-dimethyl-propionamide (9.68 g) was dissolved in 3 N hydrochloric acid (140 ml), and the solution was stirred under reflux overnight. The reaction solution was cooled to room temperature, was then washed with diethyl ether, and was neutralized with potassium carbonate powder. Diethyl ether was added thereto, and the mixture was extracted. The diethyl ether layer was dried over potassium carbonate, and the solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography using acetone-chloroform to give 2-amino-pyridine-3-carbaldehyde (5.03 g, yield 88%).

후처리

  1. temperatureunder reflux overnight
  2. washwas then washed with diethyl ether
  3. additionDiethyl ether was added
  4. extractionthe mixture was extracted
  5. dry with materialThe diethyl ether layer was dried over potassium carbonate
  6. customthe solvent was removed by distillation under the reduced pressure
  7. customThe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-ea5931a6b4484995b780c9630b52eb4d
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07560558B2

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