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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502473Generated: October 30, 2026

Trifluoroacetic acid → 7-(5-Fluoro-4-methylpyridin-3-yl)-2,6-naphthyridin-3-amine

https://huagongshe.com/reaction/1502473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 7-(5-fluoro-4-methylpyridin-3-yl)-2,6-naphthyridin-3-ylcarbamateHCID 71115017—
Solvent1,2-DichloroethaneHCID 11—
Product7-(5-Fluoro-4-methylpyridin-3-yl)-2,6-naphthyridin-3-amineHCID 67974360101.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

A suspension of tert-butyl 7-(5-fluoro-4-methylpyridin-3-yl)-2,6-naphthyridin-3-ylcarbamate (50 mg, 0.14 mmol) in 1,2-dichloroethane (1 mL) was treated with trifluoroacetic acid (0.11 mL, 1.41 mmol), and the mixture was stirred at 40° C. for 3 hours. The mixture was concentrated in vacuo and then diluted with ethyl acetate (50 mL) and washed with saturated aqueous sodium bicarbonate solution (10 mL). The organic layer was separated, dried over sodium sulfate, filtered, and evaporated in vacuo to afford the title compound as a bright yellow solid (36 mg, 98%), 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-5f1b161c463c4fccb616b58cf4c39bef
Source noteuspto-grants-2015_12