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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240Generated: October 26, 2026

Morpholine → HCID 18422066, compound

https://huagongshe.com/reaction/240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactanttert-Butyl 5-bromonicotinateHCID 18422124—
ReagentCesium carbonateHCID 10796—
CatalystBinap, (A+-)-HCID 634876—
CatalystPalladium (II) acetateHCID 4144353—
SolventTolueneHCID 1140—
ProductHCID 18422066HCID 1842206626.56%

Reaction Conditions

Temperature80 °C

Reaction Steps

tert-butyl 5-bromonicotinate (1.4 g, 5.42 mmol), morpholine (0.591 ml, 6.78 mmol), cesium carbonate (3.53 g, 10.85 mmol) and 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.507 g, 0.81 mmol) were dissolved in toluene (20 ml). The reaction flask was purged with nitrogen and diacetoxypalladium (0.061 g, 0.27 mmol) was added. The resulting suspension was stirred at 80 °C for 5 hours. The reaction mixture was diluted with EtOAc (100 mL) and washed with water (100 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 50% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford tert-butyl 5-morpholinonicotinate (0.381 g, 26.6 %) as a yellow oil which solidified on standing.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-89890e81ad5d4e12a61d2ee591f39e46
Source note750 AstraZeneca ELN dataset