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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270924Generated: October 31, 2026

methyl 3-nitro-1H-pyrazole-5-carboxylate → HCID 178498460, compound

https://huagongshe.com/reaction/270924

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 3-nitro-1H-pyrazole-5-carboxylateHCID 135452337—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178498460HCID 17849846085.4%

Reaction Steps

10.25 g (60 mmol) of 5-nitro-1H-pyrazole-3-carboxylic acid methyl ester was dissolved in 75 mL of acetic acid (AcOH) and 75 mL of tetrahydrofuran (THF). After a vacuum and argon cycle, 2.05 g (20% weight) of palladium on carbon (Pd/C 10 wt %) was added, the mixture was degassed again and filled with hydrogen from a balloon. The reaction mixture was stirred at rt under hydrogen atmosphere for 2 days. Analysis by thin layer chromatography (TLC) showed complete conversion of starting material to product. The mixture was then concentrated, the resulting purple colored oil was taken in 300 mL of ether, the finely dispersed purple impurity was filtered off, and the ether filtrate was evaporated to give 7.23 g (85% yield) of 5-amino-1H-pyrazole-3-carboxylic acid methyl ester as an off-white solid as indicated by 1H NMR; whose structure was confirmed using 1H NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449488B2
Source datasetuspto-grants-2008_11
ORD IDord-64f9b570f5094af5ac49c81562ef11f3
Source noteuspto-grants-2008_11