ChemicalBook--->CAS DataBase List--->1201935-36-5

1201935-36-5

1201935-36-5 Structure

1201935-36-5 Structure
IdentificationBack Directory
[Name]

1-(1-Methylpiperidin-4-yl)-1H-pyrazol-4-aMine
[CAS]

1201935-36-5
[Synonyms]

1-(1-methylpiperidin-4-yl)pyrazol-4-amine
1-(1-Methylpiperidin-4-yl)-1H-pyrazol-4-aMine
1-(1-methyl-4-piperidinyl)-1H-Pyrazol-4-amine
1H-Pyrazol-4-amine, 1-(1-methyl-4-piperidinyl)-
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C9H16N4
[MDL Number]

MFCD19704303
[MOL File]

1201935-36-5.mol
[Molecular Weight]

180.25
Chemical PropertiesBack Directory
[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
Spectrum DetailBack Directory
[Spectrum Detail]

1-(1-Methylpiperidin-4-yl)-1H-pyrazol-4-aMine(1201935-36-5)1HNMR
1-(1-Methylpiperidin-4-yl)-1H-pyrazol-4-aMine(1201935-36-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

Piperidine, 1-methyl-4-(4-nitro-1H-pyrazol-1-yl)-

1201935-35-4

1-(1-Methylpiperidin-4-yl)-1H-pyrazol-4-aMine

1201935-36-5

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
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