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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070632Generated: October 30, 2026

Methanol → 1-methyl-6-(3-(tetrahydro-2H-pyran-2-yloxy)prop-1-ynyl)-1H-thieno[2,3-c][1,2]thiazin-4(3H)-one 2,2-dioxide

https://huagongshe.com/reaction/1070632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetrahydro-2-(2-propynyloxy)-2H-pyranHCID 98609—
Reactant6-iodo-1-methyl-1H-thieno[2,3-c][1,2]thiazin-4(3H)-one 2,2-dioxideHCID 22397156—
CatalystTriethylamineHCID 8471—
SolventTolueneHCID 1140—
Product1-methyl-6-(3-(tetrahydro-2H-pyran-2-yloxy)prop-1-ynyl)-1H-thieno[2,3-c][1,2]thiazin-4(3H)-one 2,2-dioxideHCID 2239721266%

Reaction Steps

To a stirring mixture of 6-iodo-1-methyl-1H-thieno[2,3-c][1,2]thiazin-4(3H)-one 2,2-dioxide (Preparation 34, 1.0 g), triethylamine (1.5 mL) CuI (13.8 mg), and tetrahydro-2-(2-propynyloxy)-2H-pyran (0.49 g) in toluene (50 mL) at ambient temperature is added tetrakis triphenylphosphine palladium (40 mg). The resulting mixture is stirred overnight at ambient temperature. MeOH (50 mL) is added, the mixture is stirred 20 min and the solvent is removed in vacuo. The residue is partitioned between 10% HCl/H2O/EtOAc (100 ml each), and the organic layer is separated. The solvent is removed in vacuo and the residue purified by flash column chromatography (4/1, hexanes/EtOAc) to afford 0.68 g (66%) of the title compound as a white solid. Physical characteristics: 1H NMR (CDCl3) δ1.52-1.86, 3.39, 3.55, 3.84, 4.21, 4.45, 4.81, 7.38; MS (ESI−) m/z 354 (M−H)−. Anal. Found: C, 50.70; H, 4.89; N, 3.95.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903097B2
Source datasetuspto-grants-2005_06
ORD IDord-bbae09228bee4268904ec9df1a05ed0d
Source noteuspto-grants-2005_06