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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656527Generated: November 1, 2026

Trifluoromethanesulfonic acid → HCID 9978440, compound

https://huagongshe.com/reaction/1656527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantHCID 10414810HCID 10414810—
SolventDichloromethaneHCID 6344—
SolventAnisoleHCID 7519—
ProductHCID 9978440HCID 9978440—

Reaction Steps

To a solution of 2-[5-benzyloxycarbonylamino-6-oxo-2-(2-thienyl)-1,6-dihydro-1-pyrimidinyl]-N-(3,3,3-trifluoro-1-isopropyl-2-oxopropyl)acetamide in dichloromethane (35 mL) and anisole (1.2 mL) at 0° C. was added trifluoromethanesulfonic acid, and the resulting suspension was stirred for 15 minutes. The reaction was quenched by addition of sodium bicarbonate and the product extracted into ethyl acetate. The organic layer was washed (brine) and dried. The solvent was removed and the residue was purified by chromatography, with methanol:dichloromethane (gradient, 5:95, 7:93) as the eluent, to provide 2-[5-amino-6-oxo-2-(2-thienyl)-1,6-dihydro-1-pyrimidinyl]-N-(3,3,3-trifluoro-1-isopropyl-2-oxopropyl)acetamide as a yellow solid; 300 MHz NMR (DMSO/D2O): 7.94 (d,1), 7.65 (d,1), 7.30 (s,1), 7.22 (d,1), 7.02 (m,1), 4.84 (d,1), 4.69 (d,1), 4.07 (d,1), 2.24 (m,1), 0.89(d, 3), 0.76 (d,3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254558
Source datasetuspto-grants-1993_10
ORD IDord-229e523d1288483bb50eab2a604c6c8f
Source noteuspto-grants-1993_10