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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364305Generated: October 31, 2026

Hydrochloric Acid → 2-[2-(2,2,2-Trifluoroethyl)guanidino]-4-(4-aminobutyl)-5-methylthiazole dihydrochloride

https://huagongshe.com/reaction/364305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant2-[2-(2,2,2-Trifluoroethyl)-guanidino]-4-(4-phthalimidobutyl)-5-methylthiazole hydrochlorideHCID 21298762—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-[2-(2,2,2-Trifluoroethyl)guanidino]-4-(4-aminobutyl)-5-methylthiazole dihydrochlorideHCID 21298863128.6%

Reaction Steps

To a mixture of 2-[2-(2,2,2-trifluoroethyl)guanidino]-4-(4-phthalimidobutyl)-5-methylthiazole hydrochloride (0.60 g.) in water (2 ml.) and ethanol (2 ml.) was added sodium hydroxide pellets (0.2 g.). The resulting yellow solution was heated on a steam bath for 10 minutes and then allowed to cool to ambient temperature. The reaction mixture was adjusted to pH3 by addition of 2N hydrochloric acid and then reheated on a steam bath for 1 hour. After cooling to ambient temperature the mixture was extracted three times with equal volumes of ethyl acetate. The aqueous layer was evaporated to dryness, azeotroped twice with toluene, the residue dissolved in methanol (10 ml.) and the solution filtered. The filtrate was evaporated to dryness to give 2-[2-(2,2,2-trifluoroethyl)guanidino]-4-(4-aminobutyl)-5-methylthiazole dihydrochloride (0.31 g.) as an oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04604465
Source datasetuspto-grants-1986_08
ORD IDord-8ba06743daf647029f175c45219adf25
Source noteuspto-grants-1986_08