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| | 1-(1-Methylpiperidin-4-yl)-1H-pyrazol-4-aMine Basic information |
| Product Name: | 1-(1-Methylpiperidin-4-yl)-1H-pyrazol-4-aMine | | Synonyms: | 1-(1-Methylpiperidin-4-yl)-1H-pyrazol-4-aMine;1-(1-methyl-4-piperidinyl)-1H-Pyrazol-4-amine;1-(1-methylpiperidin-4-yl)pyrazol-4-amine;1H-Pyrazol-4-amine, 1-(1-methyl-4-piperidinyl)-;4-Amino-1-(1-Methyl-4-piperidyl)pyrazole | | CAS: | 1201935-36-5 | | MF: | C9H16N4 | | MW: | 180.25 | | EINECS: | 200-258-5 | | Product Categories: | | | Mol File: | 1201935-36-5.mol |  |
| | 1-(1-Methylpiperidin-4-yl)-1H-pyrazol-4-aMine Chemical Properties |
| Boiling point | 335.0±32.0 °C(Predicted) | | density | 1.26±0.1 g/cm3(Predicted) | | storage temp. | 2-8°C(protect from light) | | pka | 8.55±0.10(Predicted) | | Appearance | Brown to black Solid |
| | 1-(1-Methylpiperidin-4-yl)-1H-pyrazol-4-aMine Usage And Synthesis |
| Synthesis | The general procedure for the synthesis of 1-(1-methyl-4-piperidinyl)-1H-pyrazol-4-amine from the compound (CAS:1201935-35-4) was as follows: 10% Pd-C catalyst (0.1 g) was added to a solution of compound 64-b (500 mg, 2.38 mmol) in ethanol (10 mL) under an atmosphere of hydrogen (1 atm). The reaction mixture was stirred at 25 °C for 16 hours. After completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to give the reddish brown oily product 64-a (420 mg, yield: 98%). The product could be used directly in the subsequent reaction without further purification. m/z = 181 [M + H]+ from LC-MS (ESI) analysis. | | References | [1] Patent: US2015/336982, 2015, A1. Location in patent: Paragraph 0401; 0403
[2] Patent: WO2015/25197, 2015, A1. Location in patent: Paragraph 00075
[3] Patent: WO2009/153589, 2009, A1. Location in patent: Page/Page column 109
[4] Patent: US2010/317680, 2010, A1
[5] Patent: US2018/208604, 2018, A1. Location in patent: Paragraph 0339-0340 |
| | 1-(1-Methylpiperidin-4-yl)-1H-pyrazol-4-aMine Preparation Products And Raw materials |
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