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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509947Generated: November 2, 2026

Trifluoroacetic acid → HCID 57963067, compound

https://huagongshe.com/reaction/509947

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 (43, 1.50 g, 13.4 mmol) in 52.9 mL of acetonitrile, 5-fluoro-6-methoxy-pyridine-3-carbaldehyde (57, 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 (58, 3.21 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096593B2
Source datasetuspto-grants-2015_08
ORD IDord-ce3a55a1a91a4e62b748153fd6a57bf5
Source noteuspto-grants-2015_08