Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615653Generated: November 1, 2026

Trifluoroacetic acid → HCID 178425982, compound

https://huagongshe.com/reaction/1615653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1,1-Dimethylethyl (((2,4,6-trimethylphenyl)sulphonyl)oxy)carbamateHCID 359285—
Reactant1,6-Naphthyridin-5-amineHCID 29249622—
SolventDichloromethaneHCID 6344—
ProductHCID 178425982HCID 178425982—

Reaction Conditions

Temperature0 °C

Reaction Steps

To trifluoroacetic acid (10 mL), stirred at 0° C., was added tert-butyl mesitylsulfonyloxycarbamate (6.50 g, 20.6 mmol), and the mixture was stirred at 0° C. for 30 min. The mixture was poured into ice-water (10 mL). A white precipitate was formed, which was filtered and collected. The white precipitate was dissolved in DCM (20 mL), and dried with Na2SO4. To the DCM solution was added 1,6-naphthyridin-5-amine (1.0 g, 6.88 mmol), and the mixture was stirred at room temperature for 4 h. The solvent was removed under reduced pressure and the residue was washed with Et2O (3×15 mL). The yellow solid obtained was used in the next step without further purification (3.30 g). ESI MS: m/z 161 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765760B2
Source datasetuspto-grants-2014_07
ORD IDord-78d29409061b4259a66ee0da5ea22ebd
Source noteuspto-grants-2014_07