4-Aminomethyl-1-methylpyrazole

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4-Aminomethyl-1-methylpyrazole Basic information
Product Name:4-Aminomethyl-1-methylpyrazole
Synonyms:TIMTEC-BB SBB000039;AKOS PAO-0126;AKOS B000529;1-(1-METHYL-1H-PYRAZOL-4-YL)METHANAMINE;C-(1-METHYL-1H-PYRAZOL-4-YL)-METHYLAMINE;ART-CHEM-BB B000529;(1-Methyl-1H-pyrazol-4-yl)methylamine;4-Aminomethyl-1-methylpyrazole
CAS:400877-05-6
MF:C5H9N3
MW:111.15
EINECS:
Product Categories:
Mol File:400877-05-6.mol
4-Aminomethyl-1-methylpyrazole Structure
4-Aminomethyl-1-methylpyrazole Chemical Properties
Boiling point 220 °C
density 1.16
Fp 87 °C
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka8.98±0.29(Predicted)
AppearanceColorless to light yellow Liquid
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22
HazardClass IRRITANT
HS Code 2933199090
MSDS Information
4-Aminomethyl-1-methylpyrazole Usage And Synthesis
Synthesis
1H-Pyrazole-4-carboxaldehyde,1-methyl-,oxime(9CI)

43193-15-3

4-Aminomethyl-1-methylpyrazole

400877-05-6

The general procedure for the synthesis of 4-(aminomethyl)-1-methylpyrazole from the compound (CAS:43193-15-3) was as follows: the oxime 1a-k (23 mmol) was dissolved in isopropanol (100 mL), and the solution was transferred to an autoclave equipped with fluoroplastic liners. Subsequently, concentrated hydrochloric acid (10.5 mL) was added and a piece of regenerated catalyst was introduced. The hydrogenation reaction was carried out at 20 °C and 10 atm hydrogen pressure for 3-5 h, during which the reaction conditions were kept constant. The reaction process was monitored by thin layer chromatography (TLC). After complete consumption of the starting oxime, the reaction solution was poured out of the autoclave and the catalyst block was washed with methanol (3 × 30 mL), the washes were combined and mechanical impurities were removed by filtration. After evaporation of the solvent, analytically pure aromatic benzylamines 3a-k were obtained.If the hydrogenation reaction was carried out in methanol (100 mL), the solvent was removed and the residue was subsequently dried by azeotropic distillation using isopropanol (250 mL). For the hydrogenation of compound 1k, the reaction mixture is additionally reacted with activated carbon for 1 hour. The catalyst block was regenerated directly in the reactor at 400 °C in a stream of hydrogen for the subsequent hydrogenation process.

References[1] Russian Chemical Bulletin, 2018, vol. 67, # 8, p. 1394 - 1400
[2] Izv. Akad. Nauk, Ser. Khim., 2018, # 8, p. 1394 - 1400,7
4-Aminomethyl-1-methylpyrazole Preparation Products And Raw materials
Raw materials1H-Pyrazole-4-carboxaldehyde,1-methyl-,oxime(9CI)-->1-methyl-1H-pyrazole-4-carboxamide-->Hydrochloric acid-->Isopropyl alcohol-->Hydrogen
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