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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994992Generated: October 29, 2026

Thioanisole → HCID 57476393, compound

https://huagongshe.com/reaction/1994992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioanisoleHCID 7520—
ReactantTriphenylphosphine OxideHCID 13097—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67487159HCID 67487159—
SolventDichloromethaneHCID 6344—
ProductHCID 57476393HCID 5747639340.6%

Reaction Steps

To a solution of triphenylphosphine oxide (849 mg) in dichloromethane (10 mL) was added trifluoromethanesulfonic anhydride (515 μL) under ice-cooling, and the mixture was stirred for 10 min. A solution of N-[2-(benzylthio)-3,3-dimethoxypropyl]-7-[(pyridin-2-ylsulfonyl)amino]-1H-indole-2-carboxamide (1.5 g) and thioanisole (690 mg) in dichloromethane (10 mL) was added dropwise to the reaction mixture under ice-cooling, and the mixture was stirred for 10 min. Saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography to give white crystals from a fraction eluted with ethyl acetate:hexane=50:50. The white crystals were purified by preparative HPLC to give the title compound (487 mg, yield 40%) as white crystals. melting point 153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652133B2
Source datasetuspto-grants-2010_01
ORD IDord-5db8af15f1df456581fc54523deac51e
Source noteuspto-grants-2010_01