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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468956Generated: November 1, 2026

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

https://huagongshe.com/reaction/468956

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 numberUS08623889B2
Source datasetuspto-grants-2014_01
ORD IDord-67d8f3b80bec45f8ad3bb84f90eadc50
Source noteuspto-grants-2014_01