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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011714Generated: November 2, 2026

Ethyl Acetate → 3-{[2-(azetidin-1-ylcarbonyl)pyrimidin-5-yl]oxy}-5-[(1-methylethyl)oxy]-N-(1-methyl-1H-pyrazol-3-yl)benzamide

https://huagongshe.com/reaction/1011714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
Reactant2-(Azetidin-1-ylcarbonyl)-5-bromopyrimidineHCID 53629639—
Reactant3-hydroxy-5-isopropoxy-N-(1-methyl-1H-pyrazol-3-yl)benzamideHCID 59127183—
CatalystBromotris(triphenylphosphine)copper(I)HCID 11251615—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product3-{[2-(azetidin-1-ylcarbonyl)pyrimidin-5-yl]oxy}-5-[(1-methylethyl)oxy]-N-(1-methyl-1H-pyrazol-3-yl)benzamideHCID 5362953950.1%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 3-hydroxy-5-[(1-methylethyl)oxy]-N-(1-methyl-1H-pyrazol-3-yl)benzamide (250 mg, 0.91 mmol), 2-(azetidin-1-ylcarbonyl)-5-bromopyrimidine (242 mg, 1.0 mmol), cesium carbonate (886 mg, 2.72 mmol) and bromotris(triphenylphosphine)copper(I) (423 mg, 0.45 mmol) in DMA (5 mL) was stirred in a ‘Biotage initiator Microwave’ at 160° C. for 4 hours. The mixture was added to ethyl acetate (50 mL) and water (50 mL), the organic layer washed with brine (50 mL), dried (MgSO4), filtered and the solvent removed in vacuo to give a brown oil. The residue was chromatographed on silica, eluting with a gradient of 0-10% methanol in ethyl acetate, to give the desired compound (199 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977328B2
Source datasetuspto-grants-2011_07
ORD IDord-281b6afa924141fab22dde8d030bbdad
Source noteuspto-grants-2011_07