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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantMethyl 2-oxo-1,2-dihydropyridine-3-carboxylateHCID 579028—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-iodo-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 276446547%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04902796
Source datasetuspto-grants-1990_02
ORD IDord-db2dede1a70a4313a5803d1b561651a4
Source noteuspto-grants-1990_02