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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711283Generated: October 29, 2026

Trifluoroacetic acid → HCID 67208648, compound

https://huagongshe.com/reaction/711283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67208646HCID 67208646—
SolventDichloromethaneHCID 6344—
ProductHCID 67208648HCID 67208648—

Reaction Steps

To a solution of tert-butyl (1-(2-fluoroisonicotinoyl)piperidin-4-yl)methylcarbamate 93-3 (1.81 g, 5.0 mmol) in dichloromethane (10 mL) was added TFA (5 mL) dropwise at room temperature. The mixture was stirred for 10 hours, and then the solvents were removed by rotary evaporation. The residue was dissolved in ethyl acetate (100 mL), washed with saturated aqueous NaHCO3 solution, H2O and brine, dried over Na2SO4 and concentrated to dryness by rotary evaporation to give (4-(aminomethyl)piperidin-1-yl)(2-fluoropyridin-4-yl)methanone 93-4 as a yellow oil. MS m/z 238.1 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181235B2
Source datasetuspto-grants-2015_11
ORD IDord-9a8435679f2d4e0a9c93e9bbc1de6afa
Source noteuspto-grants-2015_11