N-METHYLPIPERIDINE-4-CARBOXAMIDE
N-METHYLPIPERIDINE-4-CARBOXAMIDE Basic information
- Product Name:
- N-METHYLPIPERIDINE-4-CARBOXAMIDE
- Synonyms:
-
- N-Methyl-4-piperidinecarboxaMide
- 4-Piperidinecarboxamide, N-methyl-
- N-methylpiperidin-4-carboxylic acid amide
- N-Methyl-piperidin-4-carboxamide
- CAS:
- 1903-69-1
- MF:
- C7H14N2O
- MW:
- 142.2
- Mol File:
- 1903-69-1.mol
N-METHYLPIPERIDINE-4-CARBOXAMIDE Chemical Properties
- Melting point:
- 123~125℃
- Boiling point:
- 318.5±31.0 °C(Predicted)
- Density
- 0.997±0.06 g/cm3(Predicted)
- pka
- 16.06±0.20(Predicted)
- form
- powder
- color
- Yellow
N-METHYLPIPERIDINE-4-CARBOXAMIDE Usage And Synthesis
Synthesis
544696-01-7
1903-69-1
GENERAL STEPS: 1-Boc-4-piperidinyl-N-methylamide (68 mg, 0.28 mmol) was dissolved in methanol (2 mL) and cooled to 0°C. A 1,4-dioxane solution (2 mL) of 4 M hydrogen chloride was slowly added. The reaction mixture was stirred at 0°C for 15 minutes and then gradually warmed to room temperature and continued stirring for 3 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The crude product was purified by SCX-2 column chromatography, eluting first with methanol and then with 0.5 M ammonia in methanol solution to afford N-methylpiperidine-4-carboxamide as a colorless oil (41 mg, 99% yield). The product was detected by infrared spectroscopy (CHCl3) with characteristic absorption peaks of 1308, 2948, 1663, 1525, 1227, 1119 cm-1; mass spectrometry (ESI) analysis showed that the theoretical value of the [M+H]+ ion peak of C7H15N2O was 143.1179 and the measured value was 143.1178.
References
[1] Patent: WO2010/41054, 2010, A1. Location in patent: Page/Page column 32
N-METHYLPIPERIDINE-4-CARBOXAMIDESupplier
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N-METHYLPIPERIDINE-4-CARBOXAMIDE(1903-69-1)Related Product Information
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- N-(P-ISOTHIOCYANATOPHENETHYL)SPIPERONE HYDROCHLORIDE
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- (1-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]-4-PIPERIDINYL)(MORPHOLINO)METHANONE
- N-(([(4-CHLOROBENZYL)OXY]IMINO)METHYL)-1-(2-PYRIMIDINYL)-4-PIPERIDINECARBOXAMIDE
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