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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256796Generated: October 27, 2026

Trifluoroacetic acid → 6-[(3-Chloro-pyridin-4-ylmethyl)-amino]-nicotinic acid methyl ester

https://huagongshe.com/reaction/1256796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantMethyl 6-aminonicotinateHCID 737487—
Reactant3-Chloro-4-pyridinecarboxaldehydeHCID 2762995—
SolventAcetonitrileHCID 6342—
Product6-[(3-Chloro-pyridin-4-ylmethyl)-amino]-nicotinic acid methyl esterHCID 5761929538.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To 6-amino-nicotinic acid methyl ester (553, 2.15 g, 0.014 mol) in acetonitrile (60.0 mL) were added 3-chloro-pyridine-4-carbaldehyde (554, 2.00 g, 0.014 mol), triethylsilane (11.00 mL, 0.069 mol) and trifluoroacetic acid (5.00 mL, 0.065 mol). The reaction was stirred at 80° C. overnight. The reaction was concentrated, poured into aqueous potassium carbonate, and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with 20% to 100% ethyl acetate in hexane to give the desired compound (555, 1.5 g, 38.2%). MS (ESI) [M+H+]+=278.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461169B2
Source datasetuspto-grants-2013_06
ORD IDord-776dec5c3c874a07a84e16ba9dba22d1
Source noteuspto-grants-2013_06