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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078351Generated: November 2, 2026

Hydrochloric Acid → HCID 22902388, compound

https://huagongshe.com/reaction/1078351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 135554909HCID 135554909—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
ProductHCID 22902388HCID 22902388—

Reaction Steps

100 mg of 3-{2-[N-(2-(4-chlorophenyl)-ethyl)-N-methylamino]-ethyloxy}-5-(4-hydroxyphenyl)-2-methylpyrazole (preparation see Example 9) were dissolved in 2 ml of dichloromethane. 0.15 ml of pyridine and 1 ml of acetic anhydride were added to the solution and the reaction mixture was stirred at room temperature for 24 hours. The reaction mixture was subsequently evaporated under reduced pressure, and the residue was taken up in aqueous sodium bicarbonate solution and extracted with dichloromethane. The organic phase was separated, dried and concentrated. The crude title compound which remained as a residue was taken up in tert-butyl methyl ether. To form a salt, a 2N solution of hydrochloric acid in isopropanol was added. The precipitated salt was separated. 80 mg of the hydrochloride of the title compound were obtained having a melting point of from 160° to 175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05547967
Source datasetuspto-grants-1996_08
ORD IDord-01bbc5c181e647128c8198db9b059c50
Source noteuspto-grants-1996_08