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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724622Generated: October 30, 2026

Trifluoroacetic acid → 5-{5-[(4-benzyl-4-hydroxypiperidin-1-yl)methyl]2-thienyl}-isothiazol-3(2H)-one 1,1-dioxide trifluoroacetate

https://huagongshe.com/reaction/724622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSilane, tris(1-methylethyl)-HCID 138754—
Reactant5-{5-[(4-benzyl-4-hydroxypiperidin-1-yl)methyl]2-thienyl}2-tertbutylisothiazol-3(2H)-one 1,1-dioxide trifluoroacetateHCID 69597881—
Product5-{5-[(4-benzyl-4-hydroxypiperidin-1-yl)methyl]2-thienyl}-isothiazol-3(2H)-one 1,1-dioxide trifluoroacetateHCID 2187951161%

Reaction Steps

To 4.12-B in a microwave vial was added TFA (1.9 mL) and triisopropylsilane (0.06 mL). The reaction was microwave irradiated at 130° C. for 15 min. The solvents were evaporated and crude purified by reverse phase HPLC to afford 4.12-C (11 mg, 61%). 1H NMR (500 MHz, DMSO-d6): δ 9.24 (br s, 1H), 7.52 (d, J=8 Hz, 1H), 7.31 (d, J=8 Hz, 1H), 7.23 (m, 2H), 7.17 (m, 1H), 7.14 (m, 2H), 6.67 (s, 1H), 4.80 (br s, 1H), 4.55 (d, J=7 Hz, 2H), 3.18 (m, 2H), 3.08 (m, 2H), 2.67 (s, 2H), 1.63 (m, 2H), 1.56 (m, 2H); LCMS found for C20H22N2O4S2 (M+H)+: m/z=419.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141596B2
Source datasetuspto-grants-2006_11
ORD IDord-a50fa5b83fb74e1cbe4c8dc26a09d75a
Source noteuspto-grants-2006_11