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4-Methyl-5-nitro-2-(trifluoromethyl)pyridine → 4-Methyl-6-(trifluoromethyl)pyridin-3-amine

HRID 604638
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인쇄 미리보기

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HRID 604638 반응식
[CH3:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][N:5]=[C:4]([C:11]([F:14])([F:13])[F:12])[CH:3]=1>CCO.[Pt]=O>[CH3:1][C:2]1[CH:3]=[C:4]([C:11]([F:14])([F:12])[F:13])[N:5]=[CH:6][C:7]=1[NH2:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 534142754-Methyl-5-nitro-2-(trifluoromethyl)pyridine

생성물 1

HCID 497579514-Methyl-6-(trifluoromethyl)pyridin-3-amine

시약·촉매·용매 2

HCID 82844Platinum oxide (PtO)촉매HCID 702Ethanol용매

실험 절차

A suspension of platinum oxide (36.9 mg) in a solution of 4-methyl-5-nitro-2-(trifluoromethyl)pyridine (369.4 mg, 0.162 mmol) in EtOH (12.7 mL) was stirred under a balloon of H2 for 5½ h. The reaction mixture was filtered through a plug of Celite and the filtrate was concentrated in vacuo to afford 4-methyl-6-(trifluoromethyl)pyridin-3-amine. LCMS calc.=177.1; found=177.1 (M+1)+. 1H NMR (600 MHz, CDCl3): δ 8.04 (s, 1H); 7.27 (s, 1H); 4.28 (s, 2H); 2.15 (s, 3H).

후처리

  1. filtrationThe reaction mixture was filtered through a plug of Celite
  2. concentrationthe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-8498858c1d0d4203bf9c1459721a6dba
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07910592B2

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