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| | 4-METHYL-3(2H)-PYRIDAZINONE Basic information |
| Product Name: | 4-METHYL-3(2H)-PYRIDAZINONE | | Synonyms: | 3-HYDROXY-4-METHYLPYRIDAZINE;4-methyl-2,3-dihydropyridazin-3-one;4-METHYL-3(2H)-PYRIDAZINONE;4-Methyl-pyridazin-3-ol;4-Methylpyridazin-3(2H)-one;4-Methylpyridazin-3(2H)-o...;4-Methylpyridazin-3-ol, 3-Hydroxy-4-methyl-1,2-diazine;4-Methylpyridazin-3(2H) | | CAS: | 33471-40-8 | | MF: | C5H6N2O | | MW: | 110.11 | | EINECS: | 200-001-2 | | Product Categories: | | | Mol File: | 33471-40-8.mol |  |
| | 4-METHYL-3(2H)-PYRIDAZINONE Chemical Properties |
| Melting point | 158-159 °C | | density | 1.22±0.1 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | pka | 11.51±0.40(Predicted) | | Appearance | White to off-white Solid |
| | 4-METHYL-3(2H)-PYRIDAZINONE Usage And Synthesis |
| Uses | 4-Methyl-3(2H)-pyridazinone, is used as a building block for more complex compounds. It is also found within the structure of several pharmaceutical drugs. It can be used for the synthesis of a series of aminopyridazine derivatives of γ-aminobutyric acid acting as selective GABA-A antagonists. | | Synthesis | The general procedure for the synthesis of 4-methyl-3(2H)-pyridazinone using 4-methyl-4,5-dihydropyridazin-3(2H)-one as a starting material was as follows: bromine (27.4 mL, 0.535 mol) was dissolved in glacial acetic acid (70 mL), and the solution was added slowly dropwise to 4-methyl-4,5-dihydropyridazin-3(2H)-one (25.8 g, 0.232 mol) dissolved in glacial acetic acid (330 mL), maintaining a temperature of about 50 °C during the reaction. After dropwise addition was completed, the reaction mixture was heated to 80 °C and maintained for 2 hours. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently concentrated to dryness under reduced pressure. The solid residue obtained was ground with ether and then the solid was dissolved in saturated sodium bicarbonate (NaHCO3) solution and extracted with ethyl acetate. The organic extracts were combined, dried with anhydrous sodium sulfate, filtered and concentrated to dryness under reduced pressure to give a light brown solid product (12.2 g, 48% yield). The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 11.50 (1H, s), 7.71 (1H, d, J = 4.0 Hz), 7.10 (1H, d, J = 2.8 Hz), 2.23 (3H, d, J = 1.1 Hz) ppm. | | References | [1] Patent: WO2004/74290, 2004, A1. Location in patent: Page 78-79
[2] Journal of Medicinal Chemistry, 1987, vol. 30, # 2, p. 239 - 249 |
| | 4-METHYL-3(2H)-PYRIDAZINONE Preparation Products And Raw materials |
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