Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175613Generated: October 30, 2026

Sodium Bicarbonate → 3-(Trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-5(6H)-one

https://huagongshe.com/reaction/2175613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl 5-oxo-3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylateHCID 58562753—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Product3-(Trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-5(6H)-oneHCID 58562777—

Reaction Steps

Into a 100 mL round-bottom flask, was placed a solution of tert-butyl 5-oxo-3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate (as prepared in the previous step, 2.7 g, 8.54 mmol, 1.00 equiv) in dichloromethane (20 g) and CF3COOH (4 g). The reaction mixture was stirred for 2 h at room temperature. The pH value of the solution was adjusted to 8 with sodium bicarbonate. The resulting solution was extracted with 3×30 mL of dichloromethane, and the combined organic layers was washed with 1×50 mL of brine, dried over anhydrous sodium sulfate, and concentrated under vacuum. The title compound was obtained a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062048B2
Source datasetuspto-grants-2015_06
ORD IDord-34a607a3aafc48e5b444073b9080b9b1
Source noteuspto-grants-2015_06