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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854737Generated: November 2, 2026

Formic Acid → HCID 10321174, compound

https://huagongshe.com/reaction/854737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
ReactantPotassium PermanganateHCID 516875—
ReactantHCID 21051841HCID 21051841—
SolventMethanolHCID 887—
ProductHCID 10321174HCID 1032117457.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-(4-methylsulfanyl-3-trifluoromethyl-phenyl)-N-pyrazin-2-yl-3-(tetrahydro-furan-2(R)-yl)-propionamide (0.054 g, 0.13 mmol) in formic acid (0.16 mL, 3.0 mmol) cooled to 0° C. was treated with a 30% aqueous hydrogen peroxide solution (0.08 mL, 0.65 mmol). The resulting solution was stirred at 0° C. for 30 min and was then quenched with a 10% aqueous sodium bisulfite solution. The reaction mixture was diluted with water (5 mL) and extracted with ethyl acetate (2×5 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. The resulting residue was dissolved in methanol (1 mL) and was treated dropwise with a solution of potassium permanganate (0.023 g, 0.143 mmol) in water (0.5 mL). The dark brown solution was stirred at 25° C. for 30 min and then was diluted with methanol (10 mL). The reaction mixture was filtered to remove solids, and the filtrate was concentrated in vacuo. Biotage chromatography (FLASH 12M, Silica, 7/3 hexanes/ethyl acetate to 1/1 hexanes/ethyl acetate) afforded 2-(4-methanesulfonyl-3-trifluoromethyl-phenyl)-N-pyrazin-2-yl-3-(tetrahydro-furan-2(R)-yl)-propionamide (33 mg, 57.3%) as a colorless gum: EI-HRMS m/e calcd for C19H20F3N3O4S (M)+ 443.1127. found 443.1137.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259166B2
Source datasetuspto-grants-2007_08
ORD IDord-9b4ac02cf5df45ca83a23151d9c66029
Source noteuspto-grants-2007_08