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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502416Generated: November 1, 2026

Trifluoroacetic acid → 7-Chloro-2,6-naphthyridin-3-amine

https://huagongshe.com/reaction/1502416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 7-chloro-2,6-naphthyridin-3-ylcarbamateHCID 86674971—
Solvent1,1-DichloroethaneHCID 6365—
Product7-Chloro-2,6-naphthyridin-3-amineHCID 8667497291.5%

Reaction Steps

Trifluoroacetic acid (0.43 mL, 5.5 mmol) was added to a solution of tert-butyl 7-chloro-2,6-naphthyridin-3-ylcarbamate (410 mg, 1.4 mmol) in dichloroethane (7 mL). After 4 hours, the reaction mixture was concentrated in vacuo, diluted with methylene chloride (50 mL), and washed with saturated aqueous sodium bicarbonate solution (20 mL). The organic layer was separated, dried over sodium sulfate, filtered, and evaporated in vacuo to afford a residue that was purified by flash chromatography (silica, 4 g, ISCO, 0-100% ethyl acetate in heptane) to afford the title compound as a yellow solid (230 mg, 86%), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206175B2
Source datasetuspto-grants-2015_12
ORD IDord-75f02842bc244e949c940b972dfdd587
Source noteuspto-grants-2015_12