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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34765Generated: October 26, 2026

Ammonia → 4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-(3-aminopropylthio)pyrimidine

https://huagongshe.com/reaction/34765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4-[3-(2,2,2-Trifluoroethyl)thioureido]-[(3-phthalimido)propylthio]pyrimidineHCID 86738667—
SolventDimethylformamideHCID 6228—
Product4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-(3-aminopropylthio)pyrimidineHCID 21298711—

Reaction Steps

A mixture of 4-[3-(2,2,2-trifluoroethyl)thioureido]-[(3-phthalimido)propylthio]pyrimidine (0.4 g.), N,N,-dimethylformamide (5 ml.), saturated ethanolic ammonia (10 ml.) and yellow mercuric oxide (280 mg.) was stirred at room temperature for 3 hours and then filtered and the filtrate evaporated to dryness. A solution of the residue in ethanol (10 ml.) was treated with hydrazine hydrate (1 ml.), the mixture heated under reflux for 1 hour and then evaporated to dryness. The residue was stirred with 1N hydrochloric acid and then filtered and the filtrate basified with 17N NaOH. The mixture was extracted with ether and the combined ether extracts dried and evaporated to dryness to give 4-[2-(2,2,2-trifluoroethyl)guanidino]-2-[(3-amino)propylthio]pyrimidine which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04762932
Source datasetuspto-grants-1988_08
ORD IDord-18d9153dd9ca4dda9fa425e08d3cab46
Source noteuspto-grants-1988_08