4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE
4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE Basic information
- Product Name:
- 4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE
- Synonyms:
-
- 4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE
- AURORA KA-6685
- 4-Chloro-2,3-dihydro-5-methoxy-3-oxopyridazine
- 5-chloro-4-methoxy-1H-pyridazin-6-one
- 4-Chloro-5-methoxy-3(2H)-pyridazinone
- 4-chloro-5-methoxy-2,3-dihydropyridazin-3-one
- 3(2H)-Pyridazinone, 4-chloro-5-methoxy-
- 4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE ISO 9001:2015 REACH
- CAS:
- 63910-43-0
- MF:
- C5H5ClN2O2
- MW:
- 160.56
- Product Categories:
-
- Pyrazines, Pyrimidines & Pyridazines
- Pyrazines, Pyrimidines & Pyridazines
- Mol File:
- 63910-43-0.mol
4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE Chemical Properties
- Melting point:
- 225 °C(dec.)
- Density
- 1.51±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- powder to crystal
- pka
- 8.90±0.60(Predicted)
- color
- White to Orange to Green
4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE Usage And Synthesis
Synthesis
932-22-9
124-41-4
63910-43-0
General procedure for the synthesis of 4-chloro-5-methoxypyridazin-3(2H)-one (10): to a solution of 4,5-dichloropyridazin-3(2H)-one (4.1 g, 24.8 mmol) in methanol (50 mL) was added sodium methanolate (2.6 g, 74.5 mmol). The reaction mixture was stirred at 80 °C overnight. Upon completion of the reaction, the mixture was concentrated under reduced pressure and purified by column chromatography [eluent: petroleum ether to petroleum ether/dichloromethane/methanol (10:1:1)] to afford the target product, 4-chloro-5-methoxypyridazin-3(2H)-one (10) (1.2 g, 30% yield), as a white solid. The procedure for the synthesis of 4-chloro-2-(2-chlorobenzyl)-5-methoxypyridazin-3(2H)-one (11) was not provided with complete information.
References
[1] Journal of Medicinal Chemistry, 2004, vol. 47, # 19, p. 4716 - 4730
[2] Patent: WO2015/143164, 2015, A1. Location in patent: Page/Page column 115
[3] Monatshefte fuer Chemie, 1989, vol. 120, p. 329 - 342
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