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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979747Generated: October 30, 2026

Diethyl (ethoxymethylene)malonate → HCID 20438310, compound

https://huagongshe.com/reaction/1979747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
Reactant1-benzyl-1H-pyrazol-3-amineHCID 1508616—
SolventEthanolHCID 702—
ProductHCID 20438310HCID 20438310—

Reaction Steps

1-benzyl-3-amino-pyrazole, m.p. 57°-59° C. (4 g) was reacted with diethyl ethoxymethylenemalonate (6 g) in anhydrous ethanol (40 ml) at the reflux temperature for 3 hours. After cooling the solution was evaporated in vacuo to dryness. Crystallization obtained by dilution with hexane gave diethyl N-(1-benzyl-pyrazol-3-yl)-aminomethylenemalonate, m.p. 60°-62° C. (7.5 g), which was reacted with polyphosphoric acid (3.2 g: 1.5 g of P2O5 and 1.7 g of H3PO4) and POCl3 (13.5 g) under stirring at 120° C. for 30 minutes. After cooling the reaction mixture was diluted with ice water: neutralization with 35% NaOH gave a precipitate which was filtered and washed with water. Crystallization from methanol gave 6 g of 1-benzyl-7-oxo-1H,7H-pyrazolo[1,5-a]pyrimidine-6-carboxylic acid, ethyl ester, m.p. 172°-173° C., which was hydrolized by heating with a mixture 1:1 of 37% HCl:acetic acid (300 ml) at the reflux temperature for 4 hours. After cooling the reaction mixture was neutralized to pH=6 with 35% NaOH and the precipitate was filtered and washed with water: crystallization from isopropyl alcohol gave 9.7 g of 1-benzyl-7-oxo-1H,7H-pyrazolo[1,5-a]pyrimidine-6-carboxylic acid, m.p. 198°-199° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04482555
Source datasetuspto-grants-1984_11
ORD IDord-c7c9e87a54ac4491872fe5249c43f9cd
Source noteuspto-grants-1984_11