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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473059Generated: October 27, 2026

Tetrahydrofuran → Eletriptan

https://huagongshe.com/reaction/473059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant(R)-(1-methylpyrrolidin-2-yl)(5-(2-(phenylsulfonyl)ethyl)-1H-indol-3-yl)methanoneHCID 9908745—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
ProductEletriptanHCID 7799375%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a suspension of LAH and THF was slowly charged (R)-(1-methylpyrrolidin-2-yl)(5-(2-(phenylsulfonyl)ethyl)-1H-indol-3-yl)methanone at 0° C. and then the reaction was slowly heated to reflux. Upon completion of the reaction in about 3-5 h, the reaction was cooled to 0-5° C. and 1N NaOH soln and H2O were sequentially charged. The solids were filtered and the precipitate washed with additional THF. The filtrate was distilled to dryness under reduced pressure. The residue was dissolved in water and the aqueous layer extracted with dichloromethane and dried over sodium sulfate and distilled to give the title compound in 75-80% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633239B2
Source datasetuspto-grants-2014_01
ORD IDord-0fca0fefa34d444a9f9b39b509f73dd4
Source noteuspto-grants-2014_01