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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415024Generated: November 1, 2026

N-Iodosuccinimide → HCID 135804109, compound

https://huagongshe.com/reaction/2415024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantHCID 135561638HCID 135561638—
SolventAcetonitrileHCID 6342—
ProductHCID 135804109HCID 13580410997.7%

Reaction Steps

2-Isopropylthio-6-trifluoromethyl-3H-pyrimidin-4-one (23.3 g) was dissolved in acetonitrile (230 ml) and N-iodosuccinimide (24.2 g) was added at room temperature with stirring. The mixture was refluxed for 2.5 hr and the solvent was removed under reduced pressure. The precipitates were dissolved in ethyl acetate, and then washed with aqueous sodium thiosulfate, water and brine, respectively. The ethyl acetate layer was dried over magnesium sulfite and the solvent was removed under reduced pressure to give 5-iodo-2-isopropylthio-6-trifluoromethyl-3H-pyrimidin-4-one (34.8 g) as pale yellow needles, mp 212-215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818631B1
Source datasetuspto-grants-2004_11
ORD IDord-091181a3f3a540d4b1318385e59ba461
Source noteuspto-grants-2004_11