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HCID 178418361, 화합물 → N-(4-amino-5-methylpyridin-2-yl)acetamide

HRID 537025
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HRID 537025 반응식
[CH3:1][C:2]1[C:3]([N+:13]([O-])=O)=[CH:4][C:5]([NH:9][C:10](=[O:12])[CH3:11])=[N+:6]([O-])[CH:7]=1.[H][H]>CO.[OH-].[OH-].[Pd+2]>[NH2:13][C:3]1[C:2]([CH3:1])=[CH:7][N:6]=[C:5]([NH:9][C:10](=[O:12])[CH3:11])[CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 178418361HCID 178418361, 화합물HCID 178474345HCID 178474345, 화합물

생성물 1

HCID 66747868N-(4-amino-5-methylpyridin-2-yl)acetamide수율 86.5%

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 887Methanol용매

실험 절차

A mixture of N-(5-methyl-4-nitro-1-oxidopyridin-2-yl)acetamide (3.1 g, 14.7 mmol) and Pd(OH)2 (20% on carbon, 1.6 g) in MeOH (80 mL) was allowed to stir under 40 psi of hydrogen at rt for 6 days. The reaction mixture was then filtered over celite and the filter cake was washed with DCM. The filtrate was concentrated to give N-(4-amino-5-methylpyridin-2-yl)acetamide (2.1 g, 86%) which was used without further purification.

후처리

  1. filtrationThe reaction mixture was then filtered over celite
  2. washthe filter cake was washed with DCM
  3. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-bc8f879f10754d499ec1db3f0fcd5976
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08859768B2

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