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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49008Generated: October 29, 2026

Sodium hydride → 1-Methyl-3-(3-spiro[m-dioxane-5,2'-oxiran]-2-yl-1,2-benzisothiazol-5-yl)-6-(trifluoromethyl)uracil

https://huagongshe.com/reaction/49008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-[3-[5-(Bromomethyl)-5-hydroxy-m-dioxan-2-yl]-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)uracilHCID 20634238—
SolventTetrahydrofuranHCID 8028—
Product1-Methyl-3-(3-spiro[m-dioxane-5,2'-oxiran]-2-yl-1,2-benzisothiazol-5-yl)-6-(trifluoromethyl)uracilHCID 2063419516.3%

Reaction Steps

To a mixture of 3-[3-[5-(bromomethyl)-5-hydroxy-m-dioxan-2-yl]-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)uracil (0.580 g, 1.11 mmol) and tetrahydrofuran at 5° C. is added sodium hydride (60% dispersion in mineral oil, 0.0400 g, 1.11 mmol). The resultant mixture is stirred overnight at ambient temperature and treated with additional sodium hydride (0.0400 g, 1.11 mmol). The mixture is poured into saturated ammonium chloride and extracted twice with diethyl ether. The combined organic extracts are washed with water and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue is chromatographed on silica gel with diethyl ether-methylene chloride to afford the title compound (0.0800 g, 16.3%, mp 203-206° C.) which is identified by NMR spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706663B2
Source datasetuspto-grants-2004_03
ORD IDord-d3d1cb32c80f4771a7636593fd4bfba4
Source noteuspto-grants-2004_03