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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404548Generated: October 30, 2026

Cesium carbonate → 3-(5-(4-Cyclobutyl-1,4-diazepane-1-carbonyl)pyridin-2-yloxy)benzonitrile

https://huagongshe.com/reaction/404548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant3-CyanophenolHCID 13394—
ReactantSodium HydroxideHCID 14798—
Reactant(6-Chloro-pyridin-3-yl)-(4-cyclobutyl-[1,4]diazepan-1-yl)-methanoneHCID 58076653—
Solventtert-Butyl methyl etherHCID 15413—
SolventDimethylacetamideHCID 31374—
Product3-(5-(4-Cyclobutyl-1,4-diazepane-1-carbonyl)pyridin-2-yloxy)benzonitrileHCID 23624312—

Reaction Conditions

Temperature125 °C

Reaction Steps

To a solution of (6-chloro-pyridin-3-yl)-(4-cyclobutyl-[1,4]diazepan-1-yl)-methanone (101.0 g, 343.8 mmol) in dimethylacetamide (1.1 L) was added Cs2CO3 (224 g, 687.6 mmol) and m-cyanophenol (81.9 g, 687.6 mmol). The resulting mixture was warmed to 125° C. and stirred for 20 h. After cooling to room temperature, the resulting mixture was filtered and acetic acid (1.5 L) was added to the filtrate. The resulting mixture was concentrated under reduced pressure to yield a brown residue which was taken up into MTBE (1.5 L) and 1N NaOH(aq) (1.5 L). The resulting layers were thoroughly mixed and then separated. The organic extract was dried over magnesium sulfate, filtered, and concentrated to yield the title compound as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748596B2
Source datasetuspto-grants-2014_06
ORD IDord-80205d6f699f418e953a6e26290db706
Source noteuspto-grants-2014_06