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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502479Generated: October 31, 2026

Trifluoroacetic acid → 7-(4-Methylpyridin-3-yl)-2,6-naphthyridin-3-amine

https://huagongshe.com/reaction/1502479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 7-(4-methylpyridin-3-yl)-2,6-naphthyridin-3-ylcarbamateHCID 71115140—
Solvent1,2-DichloroethaneHCID 11—
Product7-(4-Methylpyridin-3-yl)-2,6-naphthyridin-3-amineHCID 7111505199.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

A suspension of tert-butyl 7-(4-methylpyridin-3-yl)-2,6-naphthyridin-3-ylcarbamate (190 mg, 0.565 mmol) in DCE (3 mL) was treated with trifluoroacetic acid (0.437 mL, 5.65 mmol) and the mixture was stirred at 40° C. for 3 hours. The reaction 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 (133 mg, 99%), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206175B2
Source datasetuspto-grants-2015_12
ORD IDord-bb84e37f8cc54a32a6c7fc109cda5cb6
Source noteuspto-grants-2015_12