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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237314Generated: October 31, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Methyl 1-benzyl-2-oxo-1,2-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/2237314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant4-FluorobenzylamineHCID 67326—
ReactantMethyl 2-oxo-2H-pyran-3-carboxylateHCID 117704—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductMethyl 1-benzyl-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 147848279.1%

Reaction Steps

A heterogeneous mixture of methyl 2-oxo-2H-pyran-3-carboxylate (Aldrich, 2.0 g, 13 mmol, 1.0 eq) and 4-fluorobenzylamine (1.5 mL, 13 mmol, 1.0 eq) in DMF (10 ml) were stirred at room temperature for 3 h. The reaction mixture was treated with EDCI (3.4 g, 18 mmol, 1.4 eq) and DMAP (0.11 g, 9.91 mmol, 0.07 eq) at room temperature and the resulting solution was stirred for 12 h. The reaction mixture was quenched with 1N aqueous HCl and the solution was extracted with ethyl acetate (4×50 mL). The combined organic extracts were washed with 10% aqueous LiCl (3×70 mL), dried (Na2SO4), filtered and the filtrate concentrated in vacuo to afford the product (2.5 g, 73%) as a solid, that was used without further purification. 1H NMR (DMSO-d6) δ 8.17-8.20 (m, 1H), 8.03-8.05 (m, 1H), 7.38-7.46 (m, 2H), 7.16-7.22 (m, 2H), 6.37 (dd, 1H, J=6.94 Hz), 5.13 (s, 2H), 3.73 (s, 3H); HRMS(ESI+), Calcd.: 262.0879, found: 262.0885.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714138B2
Source datasetuspto-grants-2010_05
ORD IDord-6c12727d0cb3425a884052e0fa36fb00
Source noteuspto-grants-2010_05