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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522934Generated: October 27, 2026

Cesium carbonate → 3-((5-fluoro-2-(3-(4-fluorophenoxy)azetidin-1-yl)pyrimidin-4-yl)amino)-N-methylbenzamide

https://huagongshe.com/reaction/522934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactant3-(4-Fluorophenoxy)azetidineHCID 21428730—
Reactant3-((2-chloro-5-fluoropyrimidin-4-yl)amino)-N-methylbenzamideHCID 86685261—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylacetamideHCID 31374—
Product3-((5-fluoro-2-(3-(4-fluorophenoxy)azetidin-1-yl)pyrimidin-4-yl)amino)-N-methylbenzamideHCID 5337285815%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-((2-chloro-5-fluoropyrimidin-4-yl)amino)-N-methylbenzamide (500 mg, 1.78 mmoL) and 3-(4-fluorophenoxy)azetidine (298 mg, 1.78 mmol) in DMA (6 mL, 3 mL/mmoL) was added cesium carbonate (580 mg, 2.67 mmol) and the reaction was degassed for 15 min. Pd2(dba)3 (80 mg, 0.089 mmol) and BINAP (55 mg, 0.089 mmol) and the reaction was allowed to heat at 100° C. in the microwave. The reaction was quenched with water and extracted with EtOAc (2×25 mL). The organic extracts were washed with brine, dried over sodium sulfate and concentrated under reduced pressure then purified by silica gel column chromatography to give 3-((5-fluoro-2-(3-(4-fluorophenoxy)azetidin-1-yl)pyrimidin-4-yl)amino)-N-methylbenzamide (97 mg, 15%) as solid. Observed mass (M+1): 412.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334269B2
Source datasetuspto-grants-2016_05
ORD IDord-6b1b78925275455db4d91b60006eb0d2
Source noteuspto-grants-2016_05