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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364542Generated: October 26, 2026

2-(Aminomethyl)aniline → 4-amino-N-(2-aminobenzyl)-5-cyano-6-ethoxypyridine-2-carboxamide

https://huagongshe.com/reaction/1364542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Aminomethyl)anilineHCID 178096—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant4-amino-5-cyano-6-ethoxypicolinic acidHCID 11846460—
SolventDimethylacetamideHCID 31374—
Product4-amino-N-(2-aminobenzyl)-5-cyano-6-ethoxypyridine-2-carboxamideHCID 66920676—

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 2-aminobenzylamine (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) δ ppm 1.27 (t, 3H) 4.21-4.37 (m, 2H) 4.45 (q, 2H) 6.33-7.25 (m, 5H). MS (ESI) negative ion 310 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888374B2
Source datasetuspto-grants-2011_02
ORD IDord-a83518342419445bb423556d9dfc5022
Source noteuspto-grants-2011_02