Identification | Back Directory | [Name]
6-HYDROXY-3-PYRIDAZINECARBOXYLIC ACID MONOHYDRATE | [CAS]
37972-69-3 | [Synonyms]
3-hydroxypyridazine-6-car... 6-Carboxy-3(2H)-pyridazinone 1,6-dihydro-6-ox-3-darbazinate 6-Hydroxy-3-pyridazinecarboxylic acid 4-hydroxypyriMidine-2-carboxylic acid 6-oxo-1H-pyridazine-3-carboxylic acid 6-keto-1H-pyridazine-3-carboxylic acid 6-hydroxy-pyridazine-3-carboxylic acid 6-Hydroxypyridazine-3-carboxylic acid 98% 1,6-Dihydro-6-oxo-3-pyridazinecarboxylic acid 6-Oxo-1,6-dihydropyridazine-3-carboxylic acid 3-Pyridazinecarboxylic acid, 1,6-dihydro-6-oxo- 6-Hydroxy-3-pyridazinecarboxylic acid monohydrate 2,3-DIHYDRO-3-OXOPYRIDAZIN-6-CARBOXYLIC ACID, MONOHYDRATE 6-oxo-1,6-dihydropyridazine-3-carboxylic acid(SALTDATA: FREE) | [EINECS(EC#)]
675-237-1 | [Molecular Formula]
C5H6N2O4 | [MDL Number]
MFCD00052805 | [MOL File]
37972-69-3.mol | [Molecular Weight]
158.112 |
Chemical Properties | Back Directory | [Melting point ]
246 °C | [density ]
1.63±0.1 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
-2.86±0.20(Predicted) | [Appearance]
White to yellow Solid |
Hazard Information | Back Directory | [Uses]
6-Hydroxypyridazine-3-carboxylic acid is a carboxylic acid derivative and can be used as an intermediate in organic synthesis. | [Synthesis]
The general procedure for the synthesis of 6-hydroxypyridazine-3-carboxylic acid from 6-oxo-1,4,5,6-tetrahydropyridazine-3-carboxylic acid was as follows: to a solution of 6-oxo-1,4,5,6-tetrahydropyridazine-3-carboxylic acid (2.50 g, 17.59 mmol) in toluene (44 mL) was added sequentially copper acetate (450 mg, 2.48 mmol), sodium carbonate ( 7.01 g, 66.14 mmol) and pyridine (4.4 mL). The reaction mixture was stirred and mixed at room temperature, then warmed to 100 °C and stirred continuously for 16 hours. After completion of the reaction, the insoluble solid was removed by filtration and the filtrate was concentrated under reduced pressure to afford 6-oxo-1,6-dihydropyridazine-3-carboxylic acid as an off-white solid (1.80 g, 73% yield). Mass spectrometry result: m/z = 177.0 [M + H]+. | [References]
[1] European Journal of Organic Chemistry, 2013, # 27, p. 6130 - 6136 [2] Patent: US2016/376283, 2016, A1. Location in patent: Paragraph 1225; 1226 [3] Patent: CN106187910, 2016, A. Location in patent: Paragraph 0120; 0121 [4] European Journal of Medicinal Chemistry, 2017, vol. 137, p. 598 - 611 |
|
|