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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377995Generated: October 30, 2026

2-Aminothiophenol → 1-(2-Benzothiazol-2-ylmethylpiperidin-1-yl)-2,2,2-trifluoroethanone

https://huagongshe.com/reaction/2377995

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
Reactant[1-(2,2,2-Trifluoroethanoyl)piperidin-2-yl] acetic acid ethyl esterHCID 86625769—
SolventWaterHCID 962—
Product1-(2-Benzothiazol-2-ylmethylpiperidin-1-yl)-2,2,2-trifluoroethanoneHCID 23146401—

Reaction Conditions

Temperature90 °C

Reaction Steps

[1-(2,2,2-Trifluoroethanoyl)piperidin-2-yl] acetic acid ethyl ester, D28 (1.34 g) and 2-aminothiophenol (1.50 g) were suspended in polyphosphoric acid (30 ml) and heated to 90° C. for 2 h with vigorous stirring. After cooling, the reaction mixture was poured into iced water and stirred vigorously for 1 h. The aqueous solution was then extracted several times with ethyl acetate. After drying (MgSO4), the solvent was removed in vacuo and the residue chromatographed (silica gel) to afford the title compound as an oil (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470710B2
Source datasetuspto-grants-2008_12
ORD IDord-fe0a6c6294504a7884ec0b76fec06e72
Source noteuspto-grants-2008_12