HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277187Generated: October 31, 2026
Triphenylphosphine → HCID 86731246, compound
https://huagongshe.com/reaction/2277187
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamate | HCID 7023103 | — |
| Reactant | DIAD toluene | HCID 66880968 | — |
| Reactant | HCID 86731244 | HCID 86731244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86731246 | HCID 86731246 | 40.5% |
Reaction Steps
To a solution of 2-(4-(cyclopropylmethoxy)-2,5-difluorophenyl)-7-fluoro-1,3-benzoxazol-6-ol (1.34 g), tert-butyl ((2S)-1-hydroxypropan-2-yl)carbamate (1.05 g) and triphenylphosphine (1.57 g) in THF (50 mL) was added dropwise diisopropyl azodicarboxylate toluene solution (1.9 M, 3.16 mL) at 0° C., and the mixture was stirred at room temperature for 30 min. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (NH, hexane/ethyl acetate). To the obtained solid was added 4 M hydrogen chloride/ethyl acetate (10 mL), and the mixture was stirred at room temperature for 10 min, and concentrated. To the residue were added pyridine (10 mL) and acetic anhydride (10 mL), and the mixture was stirred at room temperature for 15 min. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (NH, hexane/ethyl acetate) to give the title compound (704 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133129B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-6ed56b73c2d44efebd7eef707e0c6a98 |
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| Source note | uspto-grants-2015_09 |
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