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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759405Generated: October 31, 2026

Trifluoroacetic acid → HCID 12873978, compound

https://huagongshe.com/reaction/1759405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2,3-Dihydroimidazo(2,1-b)benzothiazol-6-amineHCID 658687—
ReactantSodium borohydrideHCID 4311764—
ProductHCID 12873978HCID 12873978—

Reaction Steps

To a stirred mixture of 60 parts of trifluoroacetic acid and 4 parts of sodium borohydride are added portionwise, during a 5 hours-period, 4 parts of 2,3-dihydroimidazo[2,1-b]benzothiazol-6-amine at 30°-40° C. The reaction mixture is poured onto 300 parts of ice-water. The precipitated product is filtered off, washed with water and taken up in trichloromethane. The mixture is washed with ammonium hydroxide. The organic phase is dried, filtered and evaporated. The residue is crystallized from acetonitrile, yielding 3.3 parts of 2,3-dihydro-N-(2,2,2-trifluoroethyl)imidazo[2,1-b]benzothiazol-6-amine; mp. 211.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04340738
Source datasetuspto-grants-1982_07
ORD IDord-bdaf1945ea5445edba57808a53775307
Source noteuspto-grants-1982_07