Identification | Back Directory | [Name]
3-(Aminomethyl)-1-methylpiperidine | [CAS]
14613-37-7 | [Synonyms]
CHEMBRDG-BB 4103006 1-Methyl-3-(aminomethyl)p... 1-Methyl-3-piperidinemethanamine 3-AMINOMETHYL-1-METHYLPIPERIDINE (1-METHYLPIPERID-3-YL)METHYLAMINE 3-PIPERIDINEMETHANAMINE, 1-METHYL- N-Methyl-3-(aMinoMethyl)piperidine N-Methyl-3-(aMinoMethyl)-piperidin (1-METHYLPIPERIDIN-3-YL)METHANAMINE (1-Methylpiperidin-3-yl)methylamine C-(1-METHYL-PIPERIDIN-3-YL)-METHYLAMINE N-Methyl-3-(aMinoMethyl)piperidine 2HCl C-(1-METHYL-PIPERIDIN-3-YL)-METHYLAMINE, HCL rac 3-(Aminomethyl)-1-methyl-piperidine, 98% 1-(1-methylpiperidin-3-yl)methanamine(SALTDATA: FREE) | [Molecular Formula]
C7H16N2 | [MDL Number]
MFCD06738902 | [MOL File]
14613-37-7.mol | [Molecular Weight]
128.22 |
Chemical Properties | Back Directory | [Boiling point ]
58°C/6mm | [density ]
0.9096 g/cm3 | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
liquid | [pka]
10.12±0.29(Predicted) | [color ]
Colourless to pale yellow |
Hazard Information | Back Directory | [Synthesis]
3-(Di-tert-butoxymethylamino)-1-methylpiperidine (500 mg, 1.52 mmol) was used as raw material and dissolved in a 1,4-dioxane solution (19.75 mL) of methanol (7.5 mL) and 10% (v/v) concentrated sulfuric acid. The reaction mixture was stirred at 25°C for 0.5 hours. Methanol (300 mL) was then added and BioRad AG1-X8 resin (OH type) was added until the pH reached 10. The resin was removed by filtration and the resin was washed with methanol (2 x 200 mL). The eluates were combined and evaporated to dryness, and the residue was purified by silica gel column chromatography (30 × 2.5 cm) to afford 3-(aminomethyl)-1-methylpiperidine (69.2 mg, 35%) using 10% concentrated ammonium hydroxide in methanol solution-dichloromethane as eluent. The product characterization data were as follows: FABMS: m/z 129.1 (MH+); HRFABMS: m/z 129.1392 (MH+), calculated value C7H17N2: m/z 129.1392; 1H NMR (CDCl3) δ 0.90 (2H, m, CH2), 1.65 (2H, m, CH2), 1.72 (1H, m. CH), 1.79 (1H, m, CH2), 1.91 (1H, m, CH2), 2.30 (3H, s, NCH3), 2.64 (2H, m, CH2), 2.82 (1H, m, CH2NH2), 2.92 (1H, m, CH2NH2); 13C NMR (CDCl3) δ CH3: 46.7; CH2: 25.2, 28.0, 46.0, 36.4, 60.3; CH: 39.9. | [References]
[1] Patent: WO2004/22561, 2004, A1. Location in patent: Page 109 |
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