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14613-37-7

14613-37-7 Structure

14613-37-7 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302+H312+H332-H318
[Precautionary statements ]

P260-P280-P308+P313
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

3-(Aminomethyl)-1-methylpiperidine(14613-37-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Imidodicarbonic acid, 2-[(1-methyl-3-piperidinyl)methyl]-, 1,3-bis(1,1-dimethylethyl) ester

672324-98-0

3-(Aminomethyl)-1-methylpiperidine

14613-37-7

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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