HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374094Generated: October 30, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Methyl 1-benzyl-2-oxo-1,2-dihydropyridine-3-carboxylate
https://huagongshe.com/reaction/2374094
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | Methyl 2-oxo-2H-pyran-3-carboxylate | HCID 117704 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 1-benzyl-2-oxo-1,2-dihydropyridine-3-carboxylate | HCID 1478482 | 79.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07459562B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-5831e0b634d34d75976b0e8373bd3b52 |
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| Source note | uspto-grants-2008_12 |
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