Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161472Generated: October 29, 2026

Proton sponge → HCID 72312846, compound

https://huagongshe.com/reaction/1161472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantProton spongeHCID 88675—
ReactantSodium BicarbonateHCID 516892—
ReactantOxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
ReactantHCID 72312803HCID 72312803—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 72312846HCID 7231284651.8%

Reaction Steps

After adding 201 mg of 1,8-bis(dimethylamino)naphthalene and 138 mg of trimethyloxonium tetrafluoroborate to a solution of 150 mg of {2-(3-hydroxy-7-methoxy-2,3-dihydrobenzofuran-5-yl)-2-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylimino]-1-methylsulfanylethylidene}carbamic acid methyl ester in 3 ml of acetonitrile at 0° C., the mixture was stirred for 2 hours. Saturated aqueous sodium hydrogencarbonate was added to the reaction mixture, and extraction was performed with ethyl acetate. After washing the organic layer with water and saturated brine, it was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (80 mg) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816522B2
Source datasetuspto-grants-2010_10
ORD IDord-71f2001a6d11440399cded791e3f1b1b
Source noteuspto-grants-2010_10