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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492948Generated: October 27, 2026

Phenylacetyl isocyanate → 2-{[4-(Azetidin-1-yl)piperidin-1-yl]carbonylamino}-4-{4-[3-(2-phenylacetyl)ureido]phenoxy}pyridine

https://huagongshe.com/reaction/492948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl isocyanateHCID 12259960—
Reactant4-(4-Aminophenoxy)-2-{[4-(azetidin-1-yl)piperidin-1-yl]carbonylamino}pyridineHCID 23153403—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-{[4-(Azetidin-1-yl)piperidin-1-yl]carbonylamino}-4-{4-[3-(2-phenylacetyl)ureido]phenoxy}pyridineHCID 2315311655%

Reaction Steps

To a solution of 4-(4-aminophenoxy)-2-{[4-(azetidin-1-yl)piperidin-1-yl]carbonylamino}pyridine (62.8 mg) in tetrahydrofuran (4.0 ml) was added a solution of 2-phenylacetyl isocyanate in hexane (0.25 M, 1.71 ml) at room temperature, followed by stirring overnight. The reaction mixture was partitioned between ethyl acetate and a saturated aqueous solution of sodium hydrogencarbonate. The organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was evaporated to give a residue, which was then purified by silica gel column chromatography (Fuji Silysia NH, eluent; ethyl acetate, then ethyl acetate:methanol=98:2) to provide the titled compound (50.0 mg, 55%) as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-400c378af1a746849c962b289b24ff53
Source noteuspto-grants-2009_05