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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629748Generated: November 4, 2026

Cesium carbonate → 1-{2-Chloro-5-[(R)-1-(4-chloro-3,5-dimethyl-phenyl)-propylamino]-benzyl}-azetidine-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1629748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant(R)-1-(4-Chloro-3,5-dimethyl-phenyl)-propylamineHCID 55278509—
Reactant1-(5-Bromo-2-chloro-benzyl)azetidine-3-carboxylic acid tert-butyl esterHCID 58374422—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Solventtert-ButanolHCID 6386—
SolventEthyl AcetateHCID 8857—
Product1-{2-Chloro-5-[(R)-1-(4-chloro-3,5-dimethyl-phenyl)-propylamino]-benzyl}-azetidine-3-carboxylic acid tert-butyl esterHCID 67346198—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of INT 57 (250 mg, 0.693 mmol), amine INT 38 (137 mg, 0.693 mmol) and cesium carbonate (678 mg, 2.079 mmol) in toluene (4.5 mL) and tert-butanol (1.8 mL) was purged with argon for 10 minutes. Then, XPhos (66.1 mg, 0.139 mmol) and palladium acetate (15.56 mg, 0.069 mmol) were added, the vial was closed and heated at 100° C. for 3 hours. The reaction mixture was then diluted with EtOAc (35 mL) and washed with water and brine. The organic layer was dried over sodium sulfate, filtered and concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791100B2
Source datasetuspto-grants-2014_07
ORD IDord-0848c373235b465daf2e8b4a7bf06181
Source noteuspto-grants-2014_07