HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474440Generated: October 30, 2026
Pyridine → Methyl 6-Oxo-1-phenyl-1,6-dihydropyridine-3-carboxylate
https://huagongshe.com/reaction/1474440
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Methyl 6-oxo-1,6-dihydropyridine-3-carboxylate | HCID 416343 | — |
| Catalyst | Cupric acetate monohydrate | HCID 165397 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 6-Oxo-1-phenyl-1,6-dihydropyridine-3-carboxylate | HCID 11989075 | 56% |
Reaction Steps
Methyl-6-oxo-1,6-dihydropyridine-3-carboxylate (6.0 g, 39.22 mmol), phenylboronic acid (5.74 g, 47.06 mmol), copper(II) acetate monohydrate (11.76 g, 58.82 mmol), pyridine (6.32 mL, 78.43 mmol) and molecular sieves (4 Å, 6.0 g) in dichloromethane (100 mL) was stirred at ambient temperature for 12 hours and filtered. Standard extractive work up provided a crude residue which was purified by silica gel column chromatography (100-200 mesh) (1-2% methanol in chloroform) to give the title compound as a brown solid (5.0 g, 56%). m.p. 100-105° C.; 1H NMR (400 MHz, CDCl3) δ 3.86 (s, 3H), 6.63 (d, J=9.5 Hz, 1H), 7.36-7.55 (m, 5H), 7.91 (dd, J=2.5, 9.9 Hz, 1H), 8.23 (d, J=2.5 Hz, 1H); IR (KBr) u 3058, 2924, 2854, 1721, 1675, 1540, 1446, 1313, 1271, 1103 cm−1; MS 230 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09018232B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-4210e4144d074256af6fa5c538cd1bb2 |
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| Source note | uspto-grants-2015_04 |
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