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N,N-dimethyl-3-(6-methyl-5-nitropyridin-3-yl)prop-2-yn-1-amine → 5-[3-(Dimethylamino)propyl]-2-methylpyridin-3-amine

HRID 1672214
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HRID 1672214 반응식
[CH3:1][N:2]([CH3:16])[CH2:3][C:4]#[C:5][C:6]1[CH:7]=[N:8][C:9]([CH3:15])=[C:10]([N+:12]([O-])=O)[CH:11]=1>CCO.[Ni]>[CH3:16][N:2]([CH3:1])[CH2:3][CH2:4][CH2:5][C:6]1[CH:11]=[C:10]([NH2:12])[C:9]([CH3:15])=[N:8][CH:7]=1
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참가 물질

4

반응물 1

HCID 58476572N,N-dimethyl-3-(6-methyl-5-nitropyridin-3-yl)prop-2-yn-1-amine

생성물 1

HCID 584766405-[3-(Dimethylamino)propyl]-2-methylpyridin-3-amine수율 93%

시약·촉매·용매 2

HCID 935Nickel촉매2회HCID 702Ethanol용매3회

실험 절차

To a solution of N,N-dimethyl-3-(6-methyl-5-nitropyridin-3-yl)prop-2-yn-1-amine (3.18 g, 13.8 mmol) in EtOH (50 mL) under an atmosphere of N2 was added Raney 2800 nickel (50% water slurry; 760 mg, 4 mmol) using 5 mL of ethanol to transfer. The mixture was purged with H2 (1 atm) and allowed to stir at rt under an atmosphere of N2 for 20 h. More Raney nickel (620 mg, 3.6 mmol) was added using 5 mL of ethanol to transfer. The mixture was purged with H2 (1 atm) and allowed to stir at rt under an atmosphere of H2 for 20 h. The mixture was filtered through Celite® and the filtrate was concentrated to give 5-[3-(dimethylamino)propyl]-2-methylpyridin-3-amine (2.45 g, 93%) as a brown solid. LCMS (AAL): Rt=0.98 min, m/z=194.4 (M+H).

후처리

  1. customThe mixture was purged with H2 (1 atm)
  2. customThe mixture was purged with H2 (1 atm)
  3. stirringto stir at rt under an atmosphere of H2 for 20 h
  4. filtrationThe mixture was filtered through Celite®
  5. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-a054a0fc867a41cea0bea9e89f09fb7f
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07998952B2

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