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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910836Generated: November 2, 2026

Morpholine → HCID 67107533, compound

https://huagongshe.com/reaction/1910836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantCesium carbonateHCID 10796—
Reactant2-(4-Bromophenyl)indolizineHCID 346940—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTolueneHCID 1140—
ProductHCID 67107533HCID 6710753324.4%

Reaction Steps

To 2-(4-bromo-phenyl)-indolizine (1.2 g, 4.42 mmol) in toluene (8 mL) was added cesium carbonate (4.3 g, 13.24 mmol) and morpholine (1.15 mL, 13.24 mmol). To this was added a mixture of bis-(triphenylphosphine)-palladium (II) chloride (120 mg) and 2-dicyclohexylphosphino-2′-(N,N′-dimethylamino)biphenyl (150 mg) in toluene (10 mL). The reaction mixture was degassed for 15 min and then refluxed for 16 h under an atmosphere of argon. The cooled reaction mixture was concentrated in vacuo and the residue dissolved in dichloromethane. The organic layer was washed with water and brine solution (×2), dried over sodium sulfate, filtered and concentrated. The crude compound was purified by column chromatography over silica gel (60-120 mesh) with 80% chloroform/petroleum ether to afford 2-(4-morpholin-4-yl-phenyl)-indolizine (300 mg, 24%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604029B2
Source datasetuspto-grants-2013_12
ORD IDord-89f47e201e3749f4ad4bfbb95fd460c7
Source noteuspto-grants-2013_12