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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504835Generated: November 2, 2026

Dimethyl Sulfide → HCID 59136009, compound

https://huagongshe.com/reaction/504835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantTriphenylphosphine OxideHCID 13097—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59135872HCID 59135872—
SolventAcetonitrileHCID 6342—
ProductHCID 59136009HCID 5913600963%

Reaction Steps

To a solution of triphenylphosphine oxide (1.98 g) in acetonitrile (30 mL) was slowly added trifluoromethanesulfonic anhydride (0.60 mL) at 0° C., and the mixture was stirred for 10 min. N-{[8-(Benzylthio)-1,4-dioxaspiro[4.5]dec-8-yl]methyl}-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamide (1.45 g) and dimethylsulfide (0.52 mL) were added, and the reaction mixture was stirred at 0° C. for 30 min. Saturated aqueous sodium hydrogencarbonate was added, and the precipitated solid was collected by filtration, and washed with water. The obtained solid was washed with ethyl acetate, and dried to give the title compound (0.75 g, yield 63%) as colorless crystals. melting point 224-225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777047B2
Source datasetuspto-grants-2010_08
ORD IDord-89a8ec2020c14a09821daf9798e0312e
Source noteuspto-grants-2010_08