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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403249Generated: October 31, 2026

Trifluoroacetic acid → HCID 57963067, compound

https://huagongshe.com/reaction/1403249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
Reactant6-Fluoropyridin-2-amineHCID 2761399—
Reactant5-Fluoro-6-methoxypyridine-3-carbaldehydeHCID 44754784—
SolventAcetonitrileHCID 6342—
ProductHCID 57963067HCID 5796306799%

Reaction Conditions

Temperature80 °C

Reaction Steps

To 6-fluoro-pyridin-2-ylamine (14, 1.50 g, 13.4 mmol) in 52.9 mL of acetonitrile, 5-fluoro-6-methoxy-pyridine-3-carbaldehyde (23, 2.00 g, 12.9 mmol), triethylsilane (10.6 mL, 66.3 mmol), and trifluoroacetic acid (5.3 mL, 69.0 mmol) were added. The reaction was stirred at 80° C. overnight, then concentrated under vacuum, combined with water and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material was purified by silica gel column chromatography, eluting with 15-100% ethyl acetate in hexane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound as white solid (24, 3.21 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912204B2
Source datasetuspto-grants-2014_12
ORD IDord-02019b8b1ed2485ab786287cb6ff2e7f
Source noteuspto-grants-2014_12