ChemicalBook--->CAS DataBase List--->1191453-81-2

1191453-81-2

1191453-81-2 Structure

1191453-81-2 Structure
IdentificationBack Directory
[Name]

5-Chloro-1-Methyl-1H-pyrazol-3-aMine
[CAS]

1191453-81-2
[Synonyms]

5-Chloro-1-Methyl-1H-pyrazol-3-aMine
3-Amino-5-chloro-1-methyl-1H-pyrazole
1H-Pyrazol-3-amine, 5-chloro-1-methyl-
[Molecular Formula]

C4H6ClN3
[MOL File]

1191453-81-2.mol
[Molecular Weight]

131.56
Chemical PropertiesBack Directory
[Boiling point ]

268.0±20.0 °C(Predicted)
[density ]

1.48±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

2.99±0.11(Predicted)
[Appearance]

Light yellow to yellow Solid
[InChI]

InChI=1S/C4H6ClN3/c1-8-3(5)2-4(6)7-8/h2H,1H3,(H2,6,7)
[InChIKey]

SEVSLCCFKWIBBN-UHFFFAOYSA-N
[SMILES]

N1(C)C(Cl)=CC(N)=N1
Spectrum DetailBack Directory
[Spectrum Detail]

5-Chloro-1-Methyl-1H-pyrazol-3-aMine(1191453-81-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

1H-Pyrazole, 5-chloro-3-(2,5-dimethyl-1H-pyrrol-1-yl)-1-methyl-

89088-52-8

5-Chloro-1-Methyl-1H-pyrazol-3-aMine

1191453-81-2

5-Chloro-3-(2,5-dimethyl-1H-pyrrol-1-yl)-1-methyl-1H-pyrazole (CAS: 89088-52-8, 0.50 g, 2.38 mmol) was used as a raw material, which was dissolved in ethanol (20 mL) in a sealed tube. Subsequently, an ethanol (5 mL) solution of hydroxylamine hydrochloride (0.83 g, 12.0 mmol) was added dropwise, followed by a water (10 mL) solution of potassium hydroxide (0.30 g, 6.0 mmol) dropwise. The reaction mixture was heated at 105 °C for 2 days, during which the progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was concentrated to remove the solvent to give the crude product. The crude product was purified by silica gel column chromatography with an eluent of 0-30% ethyl acetate-hexane mixed solvent to give 5-chloro-1-methyl-1H-pyrazol-3-amine (0.29 g, 93% yield) as a yellow liquid. The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6) and mass spectrometry (MS): 1H NMR δ 5.49 (s, 1H), 4.74 (s, 2H), 3.51 (s, 3H); MS m/z: 131.94 (M + H).

[References]

[1] Patent: WO2015/25197, 2015, A1. Location in patent: Paragraph 000153
[2] Patent: US2009/264434, 2009, A1. Location in patent: Page/Page column 43
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