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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721627Generated: October 31, 2026

Triphenylphosphine → HCID 21890160, compound

https://huagongshe.com/reaction/721627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 17755504HCID 17755504—
ReactantHCID 21890637HCID 21890637—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21890160HCID 218901604.7%

Reaction Steps

4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenol (100 mg), the compound (1) (59 mg), and triphenylphosphine (106 mg) were dissolved in tetrahydrofuran (3 ml) to prepare a solution. Diethyl azodicarboxylate (0.063 ml) was then added to the solution, and the mixture was stirred at room temperature for 3 hr. The solvent was removed by distillation under the reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate, followed by washing with saturated brine. The extract was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by thin-layer chromatography using hexane/acetone for development. Diethyl ether was added to the purification product, and the precipitated crystal was collected by filtration and was washed to give the title compound (3 mg, yield 2%). Mass spectrometry value (FD-MS, m/z): 455 (M+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-957d0a302b304efd9642c576da1427c3
Source noteuspto-grants-2006_11