반응식
[NH:1]1[CH2:9][CH2:8][CH:4]([C:5]([NH2:7])=[O:6])[CH2:3][CH2:2]1.[CH2:10]=O>O.[Pd]>[CH3:10][N:1]1[CH2:9][CH2:8][CH:4]([C:5]([NH2:7])=[O:6])[CH2:3][CH2:2]1참가 물질
실험 절차
Isonipecotamide (10 g, 78.0 mmoles) was dissolved in distilled water (100 mL) and 37% aqueous formaldehyde (7.6 mL, equivalent to 2.81 g HCHO, 93.6 mmoles) was added. Wet 10% Pd—C (8 spoon spatulas) was added under argon and the mixture was hydrogenated at 25° C. and 50 psi for 43 h. The catalyst was filtered off through Celite and the latter was washed with water and methanol. The combined filtrates were evaporated to dryness and the residue was chromatographed on a silica gel column (60×5 cm) using 8%-10%-20% (10% conc. ammonium hydroxide in methanol)-dichloromethane as the eluant to give 1-methylisonipecotamide (7.15 g, 64%): FABMS: m/z 143.1 (MH+); HRFABMS: m/z 143.1184 (MH+). Calcd. for C7H15N2O: m/z 143.1184; δH (d6-DMSO) 1.50/1.57 (4H, m, CH2), 1.76/1.94 (4H, m, CH2), 2.10 (3H, s, —NCH3), 2.72 (1H, m, CH) and 6.68/7.18 ppm (2H, m, CONH2); δC (d6-DMSO) CH3, 41.2; CH2, 28.5, 28.5, 54.9, 54.9; CH, 46.2; C, 176.7.
후처리
- customwas hydrogenated at 25° C.
- filtrationThe catalyst was filtered off through Celite
- washthe latter was washed with water and methanol
- customThe combined filtrates were evaporated to dryness
- customthe residue was chromatographed on a silica gel column (60×5 cm)
출처 및 근거
- ORD 기록
- ord-05cdedd58d1f40989402cde78471bf93
- 출처 데이터셋
- uspto-grants-2010_10
- 특허 번호
- US07807683B2
연결된 노트
불러오는 중…