HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201371Generated: October 29, 2026
Triphenylphosphine → HCID 117988751, compound
https://huagongshe.com/reaction/2201371
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 | 2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamate | HCID 53384415 | — |
| Reactant | HCID 178477338 | HCID 178477338 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117988751 | HCID 117988751 | 52% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09364000B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-73c58ee2016e4528b1d5c440db721d24 |
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| Source note | uspto-grants-2016_06 |
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