3-Methylpyridazin-6-ylhydrazine
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
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
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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