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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620010Generated: November 2, 2026

Triphenylphosphine → HCID 67461046, compound

https://huagongshe.com/reaction/1620010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDibenzyl azodicarboxylateHCID 5387121—
ReactantHCID 22218487HCID 22218487—
Reactant5-ethyl-6-[2-(4-hydroxy-phenyl)-benzoxazol-6-yl]-4,5-dihydro-2H-pyridazin-3-oneHCID 136088927—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 67461046HCID 67461046—

Reaction Steps

40 mg (119 μmol) 5-ethyl-6-[2-(4-hydroxy-phenyl)-benzoxazol-6-yl]-4,5-dihydro-2H-pyridazin-3-one, 31 mg (238 μmol) 2-(ethyl-isopropyl-amino)-ethanol, 66 mg (251 μmol) triphenylphosphine and 5 ml THF are placed under protective gas. At 0° C., 58 mg (251 μmol) of DBAD are added and then the mixture is stirred overnight at RT. Then it is diluted with EA and extracted with 10% sodium carbonate solution. The organic phase is stirred with 15 mL of 4N HCl for 5 min and then extracted twice with diethyl ether. The acid H2O phase is made basic with sodium carbonate solution and extracted 3 times with DCM. The organic phase is washed with saturated saline solution and then the solv. is eliminated i.V. The residue is recrystallised with cyclohexane/EA.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772323B2
Source datasetuspto-grants-2014_07
ORD IDord-7ef1c7c56ccd4fbb8ce287085f3b655b
Source noteuspto-grants-2014_07