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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073627Generated: November 3, 2026

Methanol → Isopropyl 5-(2-aminoethoxymethyl)-3-cyano-7-(2,3-difluorophenyl)-4,7-dihydropyrazolo[1,5-a]pyrimidine-6-carboxylate hydrochloride

https://huagongshe.com/reaction/2073627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantChloroformHCID 6212—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 136364592HCID 136364592—
ProductIsopropyl 5-(2-aminoethoxymethyl)-3-cyano-7-(2,3-difluorophenyl)-4,7-dihydropyrazolo[1,5-a]pyrimidine-6-carboxylate hydrochlorideHCID 136364591—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 1.3 g of isopropyl 3-cyano-7-(2,3-difluorophenyl)-5-[2-(phthalimido)ethoxymethyl]-4,7-dihydropyrazolo[1,5-a]pyrimidine-6-carboxylate in a mixed solvent of 12 ml of methanol and 12 ml of chloroform is added 142 μl of hydrazine hydrate and the mixture is refluxed at 50° C. for 5 hours. After the solvent is distilled off, to the residue is added aqueous sodium hydrogencarbonate and then extracted with ethyl acetate. The organic layer is washed with water, dried over sodium sulfate and ethanolic hydrochloric acid is added to convert into hydrochloride. The obtained crystals are recrystallized from methanol to give 0.4 g of isopropyl 5-(2-aminoethoxymethyl)-3-cyano-7-(2,3-difluorophenyl)-4,7-dihydropyrazolo[1,5-a]pyrimidine-6-carboxylate hydrochloride 1/4 hydrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04918074
Source datasetuspto-grants-1990_04
ORD IDord-a0ec6ba8946e4a8888c856c1fd9ec0c4
Source noteuspto-grants-1990_04