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1-{[(3-Nitropyridin-2-yl)amino]methyl}-4-propylpyrrolidin-2-one → 1-{[(3-Aminopyridin-2-yl)amino]methyl}-4-propylpyrrolidin-2-one

HRID 2043605
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인쇄 미리보기

반응식

HRID 2043605 반응식
[N+:1]([C:4]1[C:5]([NH:10][CH2:11][N:12]2[CH2:16][CH:15]([CH2:17][CH2:18][CH3:19])[CH2:14][C:13]2=[O:20])=[N:6][CH:7]=[CH:8][CH:9]=1)([O-])=O>[Pd].O.CO>[NH2:1][C:4]1[C:5]([NH:10][CH2:11][N:12]2[CH2:16][CH:15]([CH2:17][CH2:18][CH3:19])[CH2:14][C:13]2=[O:20])=[N:6][CH:7]=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 577430171-{[(3-Nitropyridin-2-yl)amino]methyl}-4-propylpyrrolidin-2-one

생성물 1

HCID 577430941-{[(3-Aminopyridin-2-yl)amino]methyl}-4-propylpyrrolidin-2-one수율 113.1%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 887Methanol용매HCID 962Water용매

실험 절차

Palladium on charcoal (10% wt, 0.478 g) is added to a solution of 1-{[(3-nitropyridin-2-yl)amino]methyl}-4-propylpyrrolidin-2-one x77 (1 eq, 2.5 g, 8.983 mmol) and NH4CO2H (5 eq, 44.9 mmol, 2.832 g) in water and methanol (1/1 (v/v), 35 ml). The resulting slurry is kept under agitation during 16 hours at room temperature, then filtration over celite and evaporation of the crude mixture afford 2.524 g of 1-{[(3-aminopyridin-2-yl)amino]methyl}-4-propylpyrrolidin-2-one x78.

후처리

  1. filtrationfiltration
  2. customover celite and evaporation of the crude mixture

출처 및 근거

ORD 기록
ord-52378bd6a3d94655aee3a5fd94e4cb19
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08586623B2

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