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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620094Generated: October 25, 2026

N-Iodosuccinimide → Methyl 5-iodo-2-oxo-1,2-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/620094

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 ethyl 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-1M/S (279, M+), 247, 127 and 93.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04818819
Source datasetuspto-grants-1989_04
ORD IDord-27d5d305e56b42a5b252a99a814dddaa
Source noteuspto-grants-1989_04