1H-Pyrazole-3-carboxylicacid,4-formyl-,ethylester(9CI)

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1H-Pyrazole-3-carboxylicacid,4-formyl-,ethylester(9CI) manufacturers

1H-Pyrazole-3-carboxylicacid,4-formyl-,ethylester(9CI) Basic information
Product Name:1H-Pyrazole-3-carboxylicacid,4-formyl-,ethylester(9CI)
Synonyms:Albb-007090;ethyl 4-formyl-1H-pyrazole-3-carboxylate(SALTDATA: FREE);1H-Pyrazole-3-carboxylicacid,4-formyl-,ethylester(9CI);1H-Pyrazole-3-carboxylicacid, 4-forMyl-, ethyl ester;2H-Pyrazole-3-carboxylic acid, 4-formyl-, ethyl ester;4-Formyl-1H-pyrazole-3-carboxylic acid ethyl ester;4-formyl-2H-pyrazole-3-carboxylic acid ethyl ester;ethyl 4-formyl-2H-pyrazole-3-carboxylate
CAS:179692-09-2
MF:C7H8N2O3
MW:168.15
EINECS:
Product Categories:CARBOXYLICESTER;GLYCINESCAFFOLD;Heterocycles
Mol File:179692-09-2.mol
1H-Pyrazole-3-carboxylicacid,4-formyl-,ethylester(9CI) Structure
1H-Pyrazole-3-carboxylicacid,4-formyl-,ethylester(9CI) Chemical Properties
Boiling point 382.944±27.00 °C(Press: 760.00 Torr)(predicted)
density 1.324±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka8.874±0.10(predicted)
Safety Information
HS Code 2933199090
MSDS Information
1H-Pyrazole-3-carboxylicacid,4-formyl-,ethylester(9CI) Usage And Synthesis
Synthesis
N,N-Dimethylformamide

68-12-2

Propanoic acid,2-[2-(aminocarbonyl)hydrazinylidene]-, ethyl ester

14923-66-1

1H-Pyrazole-3-carboxylicacid,4-formyl-,ethylester(9CI)

179692-09-2

Example 55B. Synthesis of ethyl 4-formyl-1H-pyrazole-3-carboxylate: Phosphoryl chloride (14.6 g, 95 mmol) was added dropwise to dry N,N-dimethylformamide (15 mL) at 0 °C under argon protection and stirred for 30 min. Subsequently, Example 55A (2.8 g, 16 mmol) was added in batches at 0 °C. The resulting orange solution was slowly warmed to room temperature and stirred at 60 °C for 4 hours. Upon completion of the reaction, the mixture was cooled to room temperature and poured into crushed ice. The pH was adjusted with 3N NaOH solution to about 6. The mixture was heated at 60 °C for 5 min and then cooled to room temperature. After standing at room temperature overnight, the solid was collected by filtration to give the target product Example 55B (1.5 g, 55% yield). The product was analyzed by LC-MS, [M + H]+ = 169. 1H NMR (DMSO-d6, 400 MHz) δ 14.19 (br.s, 1H), 10.26 (s, 1H), 8.43 (br.s, 1H), 4.37 (q, J = 7.2 Hz, 2H), 1.34 (t, J = 7.2 Hz, 3H).

References[1] Patent: WO2010/47956, 2010, A1. Location in patent: Page/Page column 132
[2] Patent: US2016/237059, 2016, A1. Location in patent: Paragraph 0
1H-Pyrazole-3-carboxylicacid,4-formyl-,ethylester(9CI) Preparation Products And Raw materials
Raw materialsN,N-Dimethylformamide-->Propanoic acid,2-[2-(aminocarbonyl)hydrazinylidene]-, ethyl ester-->Sodium hydroxide
Preparation Products2H,6H,7H-pyrazolo[3,4-d]pyridazin-7-one
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