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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411215Generated: October 31, 2026

Iodine → 6-iodo-1-methyl-1H-thieno[2,3-c][1,2]thiazin-4(3H)-one 2,2-dioxide

https://huagongshe.com/reaction/411215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1-methyl-1H-thieno[2,3-c][1,2]thiazin-4(3H)-one 2,2-dioxideHCID 22397167—
SolventChloroformHCID 6212—
Product6-iodo-1-methyl-1H-thieno[2,3-c][1,2]thiazin-4(3H)-one 2,2-dioxideHCID 2239715643.1%

Reaction Steps

To a stirring solution of 1-methyl-1H-thieno[2,3-c][1,2]thiazin-4(3H)-one 2,2-dioxide (Preparation 33, 1.0 g) in CHCl3 (100 ml) at ambient temperature is added HgO (1.19 g) and iodine (1.17 g). The resulting mixture is stirred overnight at ambient temperature and the solids removed by filtration through diatomaceous earth. The solvent is removed in vacuo and the residue purified via flash column chromatography (4/1, hexanes/EtOAc) to afford 0.68 g (43%) of the title compound as a tan solid. Physical characteristics: 1H NMR (CDCl3) δ 3.40, 4.20, 7.53; IR (diffuse reflectance) 2986, 1675, 1664, 1505, 1478, 1405, 1338, 1327, 1275, 1245, 1177, 1158, 1129, 818, 781 cm−1; MS (EI) m/z 343 (M+). Anal. Found: C, 24.65; H, 1.82; N, 4.08.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559145B2
Source datasetuspto-grants-2003_05
ORD IDord-fb513309bdb744a6b7d38b7267ff2770
Source noteuspto-grants-2003_05