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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367372Generated: October 27, 2026

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

https://huagongshe.com/reaction/1367372

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 numberUS07893075B2
Source datasetuspto-grants-2011_02
ORD IDord-4ab3d6addb0343ab9db4c9e1cb2b5d56
Source noteuspto-grants-2011_02