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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839304Generated: November 2, 2026

N-Iodosuccinimide → 7-Iodo-5-methylimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1839304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantHCID 17773803HCID 17773803—
CatalystN-IodosuccinimideHCID 120273—
SolventDichloromethaneHCID 6344—
Product7-Iodo-5-methylimidazo[5,1-b]thiazoleHCID 22631826105.1%

Reaction Steps

5-Methylimidazo[5,1-b]thiazole (6.90 g) was dissolved in 500 ml of dichloromethane. N-Iodosuccinimide (10.6 g) was added to the solution. The mixture was stirred at room temperature for 24 hr. N-Iodosuccinimide (1.06 g) was added thereto, followed by stirring for additional one hr. The reaction solution was washed with an aqueous sodium thiosulfate solution and brine in that order, dried over anhydrous magnesium sulfate, and then filtered. The solvent was removed by distillation under the reduced pressure. The residue was dissolved in 200 ml of dichloromethane and 100 ml of ethyl acetate. Silica gel (30 g) was added to the solution. The mixture was stirred. The silica gel was removed by filtration. The filtrate was washed with 200 ml of a mixed solution of dichloromethane:ethyl acetate=2:1. The filtrate was concentrated under the reduced pressure to give 13.08 g of 7-iodo-5-methylimidazo[5,1-b]thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677331B2
Source datasetuspto-grants-2004_01
ORD IDord-59036cf0891f4f4bb8688adad5b5c976
Source noteuspto-grants-2004_01