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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201374Generated: October 29, 2026

Triphenylphosphine → HCID 117988838, compound

https://huagongshe.com/reaction/2201374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantAmmonium ChlorideHCID 25517—
ReactantBis(2-methoxyethyl) diazene-1,2-dicarboxylateHCID 22836032—
ReactantHCID 117998109HCID 117998109—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117988838HCID 11798883875%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2.13 g of 2-ethylsulfanyl-N-[2-hydroxy-5-(trifluoromethylsulfanyl)phenyl]nicotinamide, 2.14 g of DMEAD, 2.24 g of triphenylphosphine and 20 ml of THF was stirred at 50° C. for 4 hours. A saturated aqueous ammonium chloride solution was poured to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, then dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 1.52 g of 2-(2-ethylsulfanylpyridin-3-yl)-5-(trifluoromethylsulfanyl)benzoxazole (hereinafter, referred to as Compound of Present Invention 38).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364000B2
Source datasetuspto-grants-2016_06
ORD IDord-a6f3dfe2c12d42cba3509bce5b7a493f
Source noteuspto-grants-2016_06