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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875460Generated: October 26, 2026

Sodium Iodide → 1-Thioacetylmethyl-2-nitroimidazole

https://huagongshe.com/reaction/1875460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant2-NitroimidazoleHCID 10701—
ReactantDiisopropylethylamineHCID 81531—
ReactantChloromethylthioacetateHCID 53833355—
SolventAcetonitrileHCID 6342—
Product1-Thioacetylmethyl-2-nitroimidazoleHCID 86656269—

Reaction Steps

To a solution of the chloromethylthioacetate in MeCN (100 mL) was added 2-nitroimidazole (3 g), NaI (1 g) and diisopropylethyl amine (DIEA) and refluxed. A precipitate formed after 3 h. Additional DIEA (3 mL) was added to the reaction mixture and refluxed for 4 h. Volatiles were removed, EtOAc (300 mL) added to the residue, and the ensuing mixture filtered. The filtrate was washed with water, 1M aqueous citric acid, brine, and concentrated to yield a residue. The residue was separated by column chromatography using 0-90% EtOAc/Hexane as eluent to yield 1-thioacetylmethyl-2-nitroimidazole (vi, 3.15 g) that was chlorinated as described above in Example 1A to yield compound vii.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309554B2
Source datasetuspto-grants-2012_11
ORD IDord-8296122d7f0340a3a24c6d0c5a488814
Source noteuspto-grants-2012_11