Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12883Generated: October 26, 2026

2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl ester → ethyl 5-amino-1-(oxan-4-yl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/12883

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl esterHCID 78943—
ReactantSodium AcetateHCID 517045—
Reactant(Oxan-4-yl)hydrazine hydrochlorideHCID 17773358—
SolventEthanolHCID 702—
Productethyl 5-amino-1-(oxan-4-yl)-1H-pyrazole-4-carboxylateHCID 6702077492.3%

Reaction Conditions

Temperature82.5 °C

Reaction Steps

(Tetrahydro-pyran-4-yl)-hydrazine hydrochloride (1.975 g, 12.94 mmol), ethyl (ethoxymethylene)-cyanoacetate (1.958 g, 11.57 mmol) and sodium acetate (1.370 g; 16.70 mmol) were combined in ethanol (16 mL). The mixture was heated at 80-85° C. for 17 hours. After cooling to room temperature, the reaction was concentrated and the residue was partitioned between methylene chloride and water. The organic phase was separated and washed with water and then brine. Each aqueous phase was back extracted with methylene chloride. The two organic phases were combined, dried over sodium sulfate and concentrated in vacuo. The crude material was purified by flash chromatography eluting with 60-100% ethyl acetate/hexanes to give 5-amino-1-(tetrahydro-pyran-4-yl)-1H-pyrazole-4-carboxylic acid ethyl ester (2.554 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728029B2
Source datasetuspto-grants-2010_06
ORD IDord-6f68aa42048a4899b155725c5423f581
Source noteuspto-grants-2010_06