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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201371Generated: October 29, 2026

Triphenylphosphine → HCID 117988751, compound

https://huagongshe.com/reaction/2201371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantAmmonium ChlorideHCID 25517—
ReactantBis(2-methoxyethyl) diazene-1,2-dicarboxylateHCID 22836032—
Reactant2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamateHCID 53384415—
ReactantHCID 178477338HCID 178477338—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117988751HCID 11798875152%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 0.69 g of 2-ethylsulfanyl-N-(2-hydroxy-5-trifluoromethylpyridin-3-yl) nicotinamide, 0.75 g of bis(2-methoxyethyl) azodicarboxylate (hereinafter referred to as DMEAD), 0.79 g of triphenylphosphine and 7 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 sodium sulfate, and concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 0.34 g of 2-(2-ethylsulfanylpyridin-3-yl)-6-(trifluoromethyl)oxazolo[5,4-b]pyridine (hereinafter, referred to as Compound of Present Invention 32).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364000B2
Source datasetuspto-grants-2016_06
ORD IDord-73c58ee2016e4528b1d5c440db721d24
Source noteuspto-grants-2016_06