2-(Methylamino)pyridine-4-carbonitrile → (4-Aminomethyl-pyridin-2-yl)-methyl-amine
반응식
[CH3:1][NH:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][N:10]=1)[C:6]#[N:7]>CCO.[Pd]>[NH2:7][CH2:6][C:5]1[CH:8]=[CH:9][N:10]=[C:3]([NH:2][CH3:1])[CH:4]=1참가 물질
4
실험 절차
A suspension of 2-Methylamino-isonicotinonitrile (5.6 g) and Pd/C (10%, 4 g) in EtOH (150 mL) and TEA (40 mL) was placed in a 500 mL Parr Hydrogenation bottle and hydrogenated at or below 60 psi H2 pressure over night. After filtering through a pad of Celite®, the reaction mixture was concentrated in vacuo to give a yellow oil as the desired compound.
후처리
- waithydrogenated at or below 60 psi H2 pressure over night
- filtrationAfter filtering through a pad of Celite®
- concentrationthe reaction mixture was concentrated in vacuo
출처 및 근거
- ORD 기록
- ord-2460f7546b4e43cf8f1654f8fc47b63b
- 출처 데이터셋
- uspto-grants-2012_08
- 특허 번호
- US08247430B2
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