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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467495Generated: October 29, 2026

Trifluoroacetic acid → 3-Ethynyl-5-(4-(isopropylsulfonyl)phenyl)pyrazin-2-amine

https://huagongshe.com/reaction/467495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN,N-Di(Boc)-3-ethynyl-5-[4-(isopropylsulfonyl)phenyl]pyrazin-2-amineHCID 59471983—
SolventDichloromethaneHCID 6344—
Product3-Ethynyl-5-(4-(isopropylsulfonyl)phenyl)pyrazin-2-amineHCID 5467066193.2%

Reaction Steps

TFA (34.45 g, 23.28 mL, 302.1 mmol) was added to a stirred solution of tert-butyl N-tert-butoxycarbonyl-N-[3-ethynyl-5-(4-isopropylsulfonylphenyl)pyrazin-2-yl]carbamate (5 g, 9.968 mmol) in DCM (200 mL) and the reaction mixture stirred at ambient temperature for 1.5 hours. The solvent was removed in vacuo and the residue re-dissolved in DCM and stirred with saturated aqueous NaHCO3 for 30 minutes. The layers were separated and the organic layer washed with saturated aqueous NaHCO3 (×3). The combined aqueous layers were extracted with DCM (×3) and the combined organic extracts dried (MgSO4), filtered and concentrated in vacuo. The residue was triturated from DCM and precipitate isolated by filtration and dried under vacuum to give the title product as a beige solid (2.8 g, 93% Yield). 1H NMR (400.0 MHz, DMSO) δ 1.18 (d, 6H), 3.44 (t, 1H), 4.76 (s, 1H), 7.01 (s, 2H), 7.89 (d, 2H), 8.20 (d, 2H) and 8.75 (s, 1H) ppm; MS (ES+) 302.12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623869B2
Source datasetuspto-grants-2014_01
ORD IDord-c7821eb0e7f040f3b2fb739efbe406cb
Source noteuspto-grants-2014_01