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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655333Generated: October 30, 2026

Triphenylphosphine → Methyl 3-{3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]-benzyl}-2-oxo-2,3-dihydrobenzoxazole-5-carboxylate

https://huagongshe.com/reaction/655333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
ReactantMethyl 2-oxo-2,3-dihydro-1,3-benzoxazole-5-carboxylateHCID 12395109—
Reactant{3-[5-(3-Dimethylaminopropoxy)pyrimidin-2-yl]phenyl}methanolHCID 59484942—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-{3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]-benzyl}-2-oxo-2,3-dihydrobenzoxazole-5-carboxylateHCID 58486066—

Reaction Steps

1.84 g (9.5 mmol) of methyl 2-oxo-2,3-dihydrobenzoxazole-5-carboxylate and 4.75 g (14.25 mmol) of polymer-bound triphenylphosphine (3 mmol/g) are added to a solution of 3.03 g (10.45 mmol) of {3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]phenyl}methanol in 40 ml of THF. The suspension is shaken at room temperature for 30 min. The suspension is cooled in an ice bath, and 3.35 g (14.25 mmol) of di-tert-butyl-azodicarboxylate are added in portions. After the mixture has been stirred at room temperature for 24 h, a further 4.75 g (14.25 mmol) of polymer-bound triphenylphosphine (3 mmol/g) and 3.35 g (14.25 mmol) of di-tert-butyl azodicarboxylate are added, and the mixture is shaken at room temperature for a further 24 h. The reaction mixture is filtered, the filtrate is evaporated to dryness, and the residue is purified by column chromatography on silica gel, giving 947 mg of “A64”; m.p. 125° C., ESI: 463 (M+H); Rt=3.07 min (method C);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071593B2
Source datasetuspto-grants-2011_12
ORD IDord-d9437d7c069a4e3a8363d8f9eb9b0656
Source noteuspto-grants-2011_12