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3-Methylpyridazin-6-ylhydrazine

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3-Methylpyridazin-6-ylhydrazine Basic information

Product Name:
3-Methylpyridazin-6-ylhydrazine
Synonyms:
  • 3-Hydrazinyl-6-methylpyridazine
  • 3-Methylpyridazin-6-ylhydrazine
  • (6-methylpyridazin-3-yl)hydrazine
  • (6-methyl-3-pyridazinyl)hydrazine
  • 3-Methylpyridazin-6-ylhydrazine ISO 9001:2015 REACH
  • Pyridazine, 3-hydrazinyl-6-methyl-
CAS:
38956-79-5
MF:
C5H8N4
MW:
124.14
Product Categories:
  • Pyrazines, Pyrimidines & Pyridazines
Mol File:
38956-79-5.mol
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3-Methylpyridazin-6-ylhydrazine Chemical Properties

Melting point:
74-75 °C
Boiling point:
248.0±23.0 °C(Predicted)
Density 
1.31±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
pka
6.19±0.20(Predicted)
Appearance
Yellow to brown Solid
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Safety Information

HazardClass 
IRRITANT
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3-Methylpyridazin-6-ylhydrazine Usage And Synthesis

Uses

3-Hydrazinyl-6-methylpyridazine is used in preparation of 2-(3-oxo-2H,3H-[1,2,4]triazolo[4,3-b]pyridazin-2-yl)acetamide and 2-(3-oxo-[1,2,4]triazolo[4,3-a]pyrimidin-2-yl)acetamide derivatives as GPR139 receptor modulators.

Synthesis

1121-79-5

38956-79-5

General procedure for the synthesis of 3-hydrazino-6-methylpyridazine from 3-chloro-6-methylpyridazine:[Ref. Example 35] Hydrazine monohydrate (45 mL) was added to a suspension of 3-chloro-6-methylpyridazine (3.00 g) in ethanol (45 mL), and the resulting mixture was heated and refluxed for 2.5 hours. Upon completion of the reaction, the mixture was cooled in air and the solvent was subsequently removed by evaporation under reduced pressure to give a residue. The residue was purified by silica gel column chromatography using chloroform-methanol-water (7:3:1, v/v) as the lower solvent as eluent, resulting in the title compound 3-hydrazino-6-methylpyridazine (2.35 g, 81% yield) as a solid. The structure of the product was confirmed by 1H-NMR (400 MHz, DMSO-d6): δ 2.39 (3H, s), 4.20 (2H, br), 6.94 (1H, d, J = 9.3 Hz), 7.18 (1H, d, J = 9.3 Hz), 7.64 (1H, br).ESI-MS m/z: 125 ([M + H]+).

References

[1] Patent: EP1785418, 2007, A1. Location in patent: Page/Page column 53
[2] Patent: WO2008/51808, 2008, A2. Location in patent: Page/Page column 107
[3] Journal of Heterocyclic Chemistry, 1983, vol. 20, p. 1259 - 1261
[4] Journal of the Chemical Society, 1950, p. 3236,3239
[5] Patent: US2484029, 1946,

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