HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201372Generated: October 29, 2026
Triphenylphosphine → HCID 118128168, compound
https://huagongshe.com/reaction/2201372
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Bis(2-methoxyethyl) diazene-1,2-dicarboxylate | HCID 22836032 | — |
| Reactant | HCID 178477338 | HCID 178477338 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118128168 | HCID 118128168 | 69% |
Reaction Steps
A mixture of 0.69 g of 2-ethylsulfanyl-N-(2-hydroxy-5-trifluoromethylpyridin-3-yl) nicotinamide, 0.75 g of 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 anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 0.45 g of 2-(2-ethylsulfanylpyridin-3-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as Compound of Present Invention 34).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09364000B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-4978ebbab13c445aa7e1e7e9261f49da |
|---|
| Source note | uspto-grants-2016_06 |
|---|