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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453387Generated: October 25, 2026

2,5-Pyridinediamine → Methyl 3-((6-aminopyridin-3-yl)carbamoyl)-4-methylbenzoate

https://huagongshe.com/reaction/453387

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-PyridinediamineHCID 20314—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant5-(Methoxycarbonyl)-2-methylbenzoic acidHCID 22999486—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-((6-aminopyridin-3-yl)carbamoyl)-4-methylbenzoateHCID 68453452—

Reaction Steps

In a round-bottomed flask was charged 5-(methoxycarbonyl)-2-methylbenzoic acid (0.2 g, 1.0 mmol), dicloromethane (3 ml), n,n-diisopropylethylamine (0.7 ml, 4.0 mmol), HOBt (0.16 g, 1.2 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.24 g, 1.2 mmol), and 2,5-diaminopyridine (0.11 g, 1.0 mmol) in that order. The reaction mixture was stirred at RT under N2 for 18 h. The reaction was partitioned between DCM (30 ml) and brine (20 mL). The aqueous layer was back extracted with DCM (3×15 mL) and the combined DCM layer was dried (Na2SO4) and concentrated. The crude product was dissolved in MeOH and absorbed on silica gel, pyrified by chromatography through a Redi-Sep 40 g column, eluting with a gradient of 0% to 10% MeOH in CH2Cl2, to provide methyl 3-((6-aminopyridin-3-yl)carbamoyl)-4-methylbenzoate as a tan solid. MS (ESI, pos. ion) m/z: 286.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492404B2
Source datasetuspto-grants-2013_07
ORD IDord-de5888cc3dfe4f2991bdaf9e33e27356
Source noteuspto-grants-2013_07