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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154Generated: October 23, 2026

Hydrochloric Acid → Ethyl 4-amino-5-mesityl-1-methyl-1H-pyrazole-3-carboxylate

https://huagongshe.com/en/reaction/1154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethylhydrazineHCID 6061—
ReactantHCID 178418386HCID 178418386—
SolventMethanolHCID 887—
ProductEthyl 4-amino-5-mesityl-1-methyl-1H-pyrazole-3-carboxylateHCID 1551666678.9%

Reaction Steps

To a solution of the product of step B (4.0 g, 13.8 mmol) and 1.6 mL of 12N hydrochloric acid in 100 mL of methanol was added dropwise 0.63 g of methyl hydrazine at 0° C. The reaction mixture was stirred at room temperature 4 hours, and then concentrated. The resulting residue was partitioned between water and ethyl acetate. The organic phase was separated and washed once with brine. The ethyl acetate solution was then mixed with 100 mL of water. Solid Na2S2O4 in excess was added in small portion until TLC showed completion of the reduction. The organic phase was separated, washed with water and brine, and dried over Na2SO4. Evaporation gave 3.1 g of the title compound as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723608
Source datasetuspto-grants-1998_03
ORD IDord-75a3caa0644f40ee90d13cb00258ca5f
Source noteuspto-grants-1998_03