6-CHLORO-3-OXO-2,3-DIHYDROPYRIDAZINE-4-CARBOXYLIC ACID
6-CHLORO-3-OXO-2,3-DIHYDROPYRIDAZINE-4-CARBOXYLIC ACID Basic information
- Product Name:
- 6-CHLORO-3-OXO-2,3-DIHYDROPYRIDAZINE-4-CARBOXYLIC ACID
- Synonyms:
-
- 6-chloro-3-hydroxypyridazine-4-carboxylicacid
- 4-Pyridazinecarboxylic acid, 6-chloro-2,3-dihydro-3-oxo-
- 3-chloro-6-oxo-1H-pyridazine-5-carboxylicaci
- 6-CHLORO-3-OXO-2,3-DIHYDROPYRIDAZINE-4-CARBOXYLIC ACID ISO 9001:2015 REACH
- 3-chloro-6-oxo-1H-pyridazine-5-carboxylic acid
- CAS:
- 50681-26-0
- MF:
- C5H3ClN2O3
- MW:
- 174.54
- Mol File:
- 50681-26-0.mol
6-CHLORO-3-OXO-2,3-DIHYDROPYRIDAZINE-4-CARBOXYLIC ACID Chemical Properties
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- Appearance
- White to off-white Solid
6-CHLORO-3-OXO-2,3-DIHYDROPYRIDAZINE-4-CARBOXYLIC ACID Usage And Synthesis
Uses
6-Chloro-3-hydroxypyridazine-4-carboxylic acid
Synthesis
286946-24-5
50681-26-0
A. Methyl 3,6-dichloropyridazine-4-carboxylate (2.00 g, 10.4 mmol) was dissolved in dioxane (9.0 mL) and 1M hydrochloric acid solution (10.4 mL) was added. The reaction mixture was stirred at 90°C for 20 hours. After completion of the reaction, the mixture was cooled to 0 °C and the precipitate was collected by filtration. The precipitate was washed with cold water followed by a small amount of pyridazine acid Z.1 to afford the target product 3-oxo-6-chloro-2,3-dihydropyridazine-4-carboxylic acid (955 mg, 53% yield). The product was confirmed by HPLC-MS analysis (MS (MH)+ = 173; retention time t Ret = 0.00min; analytical method: LCMSBAS1).
References
[1] Patent: WO2011/131741, 2011, A1. Location in patent: Page/Page column 62-63
[2] Patent: WO2011/144622, 2011, A1. Location in patent: Page/Page column 55
[3] Patent: US2012/94976, 2012, A1. Location in patent: Page/Page column 33-34
6-CHLORO-3-OXO-2,3-DIHYDROPYRIDAZINE-4-CARBOXYLIC ACIDSupplier
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