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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039765Generated: October 30, 2026

Triphenylphosphine → tert-Butyl 2-{4-[5-(2-fluorophenoxy)oxazolo[5,4-b]pyridin-2-yl]-2,6-dimethylphenoxy}-2-methylpropionate

https://huagongshe.com/reaction/2039765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl 2-hydroxyisobutyrateHCID 118940—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4-[5-(2-Fluorophenoxy)oxazolo[5,4-b]pyridin-2-yl]-2,6-dimethylphenolHCID 136413238—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Producttert-Butyl 2-{4-[5-(2-fluorophenoxy)oxazolo[5,4-b]pyridin-2-yl]-2,6-dimethylphenoxy}-2-methylpropionateHCID 71204480—

Reaction Steps

With ice cooling, 72 mg of triphenylphosphine were dissolved in 1 ml of dry tetrahydrofuran, and 47 mg of diethyl azodicarboxylate were added. After 15 min, 80 mg of 4-[5-(2-fluorophenoxy)oxazolo[5,4-b]pyridin-2-yl]-2,6-dimethylphenol were added, followed by 32 μl of triethylamine and 44 mg of tert-butyl alpha-hydroxyisobutyrate. The reaction mixture was then stirred at room temperature for 16 hours, and another 72 mg of triphenylphosphine and 47 mg of diethyl azodicarboxylate were added with ice cooling. After a further 4 h at room temperature, the reaction was concentrated and purified by preparative HPLC. This gave 60 mg (53%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580816B2
Source datasetuspto-grants-2013_11
ORD IDord-f8cfbaf7b8b4454684fd29f9c0eebaa8
Source noteuspto-grants-2013_11