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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814081Generated: November 3, 2026

Hexamethylphosphoramide → 2-(4-hydroxytetrahydro-4H-4-pyranyl)-5-methylthio-1-benzenesulfonylindole

https://huagongshe.com/reaction/1814081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethylphosphoramideHCID 12679—
ReactantAmmonium ChlorideHCID 25517—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
Reactant1-Benzenesulfonyl-5-methylthioindoleHCID 22504427—
SolventTetrahydrofuranHCID 8028—
SolventButyllithiumHCID 178418339—
Product2-(4-hydroxytetrahydro-4H-4-pyranyl)-5-methylthio-1-benzenesulfonylindoleHCID 22504437—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 5-methylthio-1-benzenesulfonylindole (200 mg) in tetrahydrofuran (5 ml), n-butyl lithium (0.49 ml, 1.61 M) was added at −78° C. under nitrogen atmosphere and the mixture was stirred at −78° C. for 30 minutes, followed by addition of hexamethylphosphoric triamide (0.23 ml), and the mixture was stirred for 15 minutes. Subsequently, tetrahydro-4H-pyran-4-one (0.12 ml) was added thereto and the mixture was stirred at −78° C. for 15 minutes and heated to 15 to 30° C. The reaction solution was then poured into a saturated aqueous ammonium chloride solution, extracted with dichloromethane, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was separated using silica gel preparative thin-layer chromatography (hexane:ethyl acetate=1:1) and (methanol:chloroform=1:20) to obtain 39 mg of the desired product as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875770B2
Source datasetuspto-grants-2005_04
ORD IDord-2e783a9a069d40e299e0819c292a4277
Source noteuspto-grants-2005_04