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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748529Generated: October 31, 2026

Cesium carbonate → 5-Methyl-6-[4-(morpholin-4-yl)cyclohex-1-en-1-yl]pyridin-3-amine

https://huagongshe.com/reaction/1748529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantAcetylacetoneHCID 31261—
ReactantAzane;hydrateHCID 12896473—
Reactant4-[4-(5-Bromo-3-methylpyridin-2-yl)cyclohex-3-en-1-yl]morpholineHCID 86692479—
CatalystBis(2,4-pentanedionato)copper(II)HCID 25949—
SolventDimethylformamideHCID 6228—
Product5-Methyl-6-[4-(morpholin-4-yl)cyclohex-1-en-1-yl]pyridin-3-amineHCID 86692478—

Reaction Conditions

Temperature100 °C

Reaction Steps

Acetylacetone (0.31 ml) and 28% ammonia water (1.78 ml) were added to a suspension of 4-[4-(5-bromo-3-methylpyridin-2-yl)cyclohex-3-en-1-yl]morpholine (2 g), copper acetylacetonate (466 mg) and cesium carbonate (3.86 g) in N,N-dimethylformamide (12 ml), sealed in a tube under nitrogen atmosphere and stirred at 100° C. for 20 hours. After completion of the reaction, the reaction solution was left stand to room temperature and concentrated. The resulting residue was diluted with water and extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated. The resulting residue was purified with silica gel column chromatography (chlorofolin/methanol) to give the titled compound (1.31 g) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-849469cc25c44838980b3b80b07f071e
Source noteuspto-grants-2015_10