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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277187Generated: October 31, 2026

Triphenylphosphine → HCID 86731246, compound

https://huagongshe.com/reaction/2277187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamateHCID 7023103—
ReactantDIAD tolueneHCID 66880968—
ReactantHCID 86731244HCID 86731244—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86731246HCID 8673124640.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-6ed56b73c2d44efebd7eef707e0c6a98
Source noteuspto-grants-2015_09