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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522922Generated: October 30, 2026

Cesium carbonate → 3-(6-(3-(4-fluorophenoxy)azetidin-1-yl)pyridin-2-ylamino)-N-methylbenzamide

https://huagongshe.com/reaction/522922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantDimethylacetamideHCID 31374—
Reactant4-Amino-N-methylbenzamideHCID 235516—
ReactantBinap, (A+-)-HCID 634876—
Reactant2-Chloro-6-(3-(4-fluorophenoxy)azetidin-1-yl)pyridineHCID 86685258—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product3-(6-(3-(4-fluorophenoxy)azetidin-1-yl)pyridin-2-ylamino)-N-methylbenzamideHCID 6735559513%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 2-chloro-6-(3-(4-fluorophenoxy) azetidin-1-yl)pyridine (500 mg, 1.79 mmoL) and 4-amino-N-methylbenzamide (270 mg, 1.79 mmol) in dimethylacetamide (5 mL, 3 mL/mmol) was added cesium carbonate (873 mg, 2.68 mmol) and the reaction was degassed for 15 min. Pd2(dba)3 (81 mg, 0.089 mmol) and BINAP (55 mg, 0.089 mmol) were added and the reaction was allowed to heat at 120° C. in the microwave. The reaction was quenched with water and extracted with EtOAc (2×50 mL). The organic extracts were washed with brine, dried over sodium sulfate, concentrated under reduced pressure and purified by silica gel column chromatography to afford 3-(6-(3-(4-fluorophenoxy) azetidin-1-yl)pyridin-2-ylamino)-N-methylbenzamide (61 mg, 13%) as a solid. Observed mass (M+1): 393.1. The following compounds were prepared as described in Example V above using appropriate starting materials.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334269B2
Source datasetuspto-grants-2016_05
ORD IDord-eee1e11f6b46466aa9bba959a9aea0bb
Source noteuspto-grants-2016_05