HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199805Generated: October 27, 2026
N-Iodosuccinimide → Methyl 5-iodo-2-oxo-1,2-dihydropyridine-3-carboxylate
https://huagongshe.com/reaction/1199805
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Methyl 2-oxo-1,2-dihydropyridine-3-carboxylate | HCID 579028 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-iodo-2-oxo-1,2-dihydropyridine-3-carboxylate | HCID 2764465 | 47% |
Reaction Steps
A solution containing 19.48 g of methyl 2-oxo-1,2-dihydro-3-pyridinecarboxylate and 36.15 g of N-iodosuccinimide in 500 ml of anhydrous methylene chloride is heated at reflux under a nitrogen atomosphere in the dark for 48 hours. The reaction mixture is concentrated to 150 ml under reduced pressure and the solid which forms is collected by filtration and washed with small portions of cold methylene chloride and benzene to give 16.59 g (47%) of methyl 5-iodo-2-oxo-1,2-dihydro-3-pyridinecarboxylate as a pale yellowish solid. This material is sufficiently pure for the next reaction; its properties upon recrystallization from methyl acetate are as follows: m.p. 190°-192° C.; NMR (DMSO-d6, 300 MHz) delta 3.71 (s, 3H), 7.93 (d, 1H, J=2.26 Hz), 8.10 (d, 1H, J=2.26 Hz), IR (KBr) 2500-3050 (broad), 1725, 1630, 1585, 1475, 1425, 1320, 1260, 1235, 1180, 1150, 1105, 1065, 965, 875 and 800 cm-1 ; M/S (279, M+), 247, 127 and 93.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04902796 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-db2dede1a70a4313a5803d1b561651a4 |
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| Source note | uspto-grants-1990_02 |
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