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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364541Generated: October 29, 2026

4-Methylbenzylamine → 4-amino-5-cyano-6-ethoxy-N-(4-methylbenzyl)pyridine-2-carboxamide

https://huagongshe.com/reaction/1364541

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylbenzylamineHCID 66035—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant4-Amino-5-cyano-6-ethoxypicolinic acidHCID 11846460—
SolventDimethylacetamideHCID 31374—
Product4-amino-5-cyano-6-ethoxy-N-(4-methylbenzyl)pyridine-2-carboxamideHCID 66920561—

Reaction Steps

In a 20 mL scintillation vial, 4-amino-5-cyano-6-ethoxy-pyridine-2-carboxylic acid (19 mg, 0.09 mmol) was dissolved in DMA (0.7 mL). Then TBTU (30 mg, 0.09 mmol) dissolved in DMA (0.7 mL) was added, followed by the addition of 4-methylbenzylamine (12 mg, 0.11 mmol, 1.2 eq.) in DMA (0.6 mL). Then TEA (9.37 mg, 0.09 mmol) dissolved in DMA (0.7 mL) was added. The reaction mixture was shaken at room temperature for 24 hours. The crude mixture was purified using reverse phase HPLC (TFA). 1H NMR (500 MHz, DMSO-D6/D2O) 1.23-1.36 (m, 3H) 2.20-2.34 (m, 3H) 4.37-4.55 (m, 4H) 7.04-7.22 (m, 4H) 8.97-9.10 (m, 1H). MS (ESI) positive ion 311 (M+H)+; negative ion 309 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888374B2
Source datasetuspto-grants-2011_02
ORD IDord-224d4256a47b47edb5e67587ce9d8f44
Source noteuspto-grants-2011_02