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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642374Generated: November 1, 2026

Iodine → 6-Iodo-7-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one

https://huagongshe.com/reaction/1642374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant7-Methyl-5H-(1,3)thiazolo(3,2-a)pyrimidin-5-oneHCID 597065—
ReactantHCID 66753972HCID 66753972—
SolventAcetonitrileHCID 6342—
Product6-Iodo-7-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-oneHCID 66753571—

Reaction Steps

A stirred solution of Step 1 Intermediate (20 g, 120.463 mmol) in acetonitrile (200 ml) was treated with ceric ammonium nitrate (33 g, 60.233 mmol) and iodine (18 g, 72.281 mmol) at room temperature according to the procedure outlined in Intermediate 1, Step 3 to give 35 g of the product as a light yellow solid; 1H NMR (300 MHz, DMSO-d6) δ 2.56 (s, 3H), 7.52 (d, J=5.1 Hz, 1H), 7.97 (d, J=4.8 Hz, 1H); ESI-MS (m/z) 291.29 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119647B2
Source datasetuspto-grants-2012_02
ORD IDord-ed55976fa2264f37944e536d84f6d7b5
Source noteuspto-grants-2012_02