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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443114Generated: November 3, 2026

N-Iodosuccinimide → 7-Iodo-2-methyl-5H-thiazolo[4,5-c]pyridin-4-one

https://huagongshe.com/reaction/1443114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant2-Methyl-5H-thiazolo[4,5-c]pyridin-4-oneHCID 68540979—
SolventAcetonitrileHCID 6342—
Product7-Iodo-2-methyl-5H-thiazolo[4,5-c]pyridin-4-oneHCID 68538257—

Reaction Conditions

Temperature5 °C

Reaction Steps

2-Methyl-5H-thiazolo[4,5-c]pyridin-4-one (770 mg, 4.6 mmol) was suspended in 25 ml acetonitrile and N-iodosuccinimide (1.04 g, 4.6 mmol) was added. The reaction mixture was refluxed for 3 hrs. The brown suspension was cooled to 5° C. and stirred for 15 min. The solid was filtered, washed with cold acetonitrile and dried for 1 hour at 50° C. and <30 mbar. The crude product (830 mg, 61%) [MS: m/e=292.9 (M+H+)] was used without any further purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659401B2
Source datasetuspto-grants-2010_02
ORD IDord-ab41380a4b9b4e1cb3eca0d41b2332df
Source noteuspto-grants-2010_02