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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517366Generated: October 28, 2026

ethyl 3-chloro-1-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-5-carboxylate → ethyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/517366

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 3-chloro-1-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-5-carboxylateHCID 118021759—
CatalystHCID 178418406HCID 178418406—
SolventAcetonitrileHCID 6342—
Productethyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylateHCID 118022610—

Reaction Conditions

Temperature60 °C

Reaction Steps

In a preferred reaction, ethyl 3-chloro-1-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-5-carboxylate (10b) and acetonitrile are mixed with manganese(IV) oxide and the mixture is heated at about 60° C. until the reaction is completed. The ethyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylate (10c) is conveniently isolated and purified by standard techniques.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115115B1
Source datasetuspto-grants-2015_08
ORD IDord-a8ab26a2ca434c94874c1ace3b9e5bc7
Source noteuspto-grants-2015_08