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N-Methyl-3-nitro-5-(trifluoromethyl)pyridin-2-amine → N2-Methyl-5-(trifluoromethyl)pyridine-2,3-diamine

HRID 533655
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인쇄 미리보기

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HRID 533655 반응식
[CH3:1][NH:2][C:3]1[C:8]([N+:9]([O-])=O)=[CH:7][C:6]([C:12]([F:15])([F:14])[F:13])=[CH:5][N:4]=1.[H][H]>[C].[Pd].C(O)C>[CH3:1][NH:2][C:3]1[C:8]([NH2:9])=[CH:7][C:6]([C:12]([F:15])([F:13])[F:14])=[CH:5][N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 2775319N-Methyl-3-nitro-5-(trifluoromethyl)pyridin-2-amineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 2735930N2-Methyl-5-(trifluoromethyl)pyridine-2,3-diamine수율 83.8%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 702Ethanol용매

실험 절차

A mixture of N-methyl-(3-nitro-5-trifluoromethyl-pyridin-2-yl)-amine (6.93 g), 5% of palladium-carbon (0.69 g), and ethanol was stirred under about 1 atm of hydrogen at room temperature for 10 hours. The reaction mixture was filtered through Celite®, and then the filtrate was concentrated under reduced pressure to give 5.02 g of N2-methyl-5-trifluoromethylpyridin-2,3-diamine (Compound (1F)-1).

후처리

  1. filtrationThe reaction mixture was filtered through Celite®
  2. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-4e2fb92a64fe4c21aa8d9a761ed94fa7
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08853238B2

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