N-(1-Methyl-4-piperidinyl)-5-nitro-2-pyrimidinamine → HCID 24823424, 화합물

HRID 453359노트

반응식

HRID 453359 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([NH:8][C:9]2[N:14]=[CH:13][C:12]([N+:15]([O-])=O)=[CH:11][N:10]=2)[CH2:4][CH2:3]1>CCOC(C)=O.CO.[Pd]>[CH3:1][N:2]1[CH2:3][CH2:4][CH:5]([NH:8][C:9]2[N:10]=[CH:11][C:12]([NH2:15])=[CH:13][N:14]=2)[CH2:6][CH2:7]1

참가 물질

5

반응물 1

HCID 24823901N-(1-Methyl-4-piperidinyl)-5-nitro-2-pyrimidinamine

생성물 1

HCID 24823424HCID 24823424, 화합물

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 887Methanol용매HCID 8857Ethyl Acetate용매

실험 절차

The crude N-(1-methylpiperidin-4-yl)-5-nitropyrimidin-2-amine was combined with 10% Pd/C (500 mg) in EtOAc (8 mL) and MeOH (20 mL) was added. The mixture was purged with H2 and allowed to stir under 1 atm H2 overnight. Filtration through a pad of celite and concentration afforded N2-(1-methylpiperidin-4-yl)pyrimidine-2,5-diamine 17 as a tan solid, which may be used without further purification. MS: m/z found 285 [MH+].

후처리

  1. additionwas added
  2. customThe mixture was purged with H2
  3. filtrationFiltration
  4. concentrationthrough a pad of celite and concentration

출처 및 근거

ORD 기록
ord-2174d5e7dc5b4a4ca04a4f702a9ef91b
출처 데이터셋
uspto-grants-2013_07
특허 번호
US08492404B2

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