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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443899Generated: October 30, 2026

Trifluoroacetic acid → HCID 12873978, compound

https://huagongshe.com/reaction/443899

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 numberUS04262004
Source datasetuspto-grants-1981_04
ORD IDord-4ab475c3118f4cb98f077b31627c48ee
Source noteuspto-grants-1981_04