Morpholine → HCID 57422999, compound

HRID 416Notes

Reaction equation

HRID 416 reaction equation
C1COCCN1.COC(=O)c1cc(Br)c(OC)cc1Cl>CC(=O)O.CC(=O)O.Cc1ccccc1.O=C([O-])[O-].[Cs+].[Cs+].[Pd].c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1>COC(=O)c1cc(N2CCOCC2)c(OC)cc1Cl

Participants

7

Conditions

Temperature
100 °C

Procedure

Palladium(II) acetate (0.040 g, 0.18 mmol), methyl 2-chloro-4-methoxy-5-morpholinobenzoate (2.042 g, 80 %), cesium carbonate (4.08 g, 12.52 mmol) and racemic 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.223 g, 0.36 mmol) were mixed together in a round bottom flask and evacuated then purged with nitrogen. Morpholine (0.780 mL, 8.94 mmol) and degassed toluene (15 mL) were added and the resulting suspension (orange/red) was degassed and purged with nitrogen 3 times. The mixture was heated to 100 °C under nitrogen overnight. The mixture was allowed to cool to ambient temperature and filtered, washing with EtOAc. The filtrate was concentrated and the crude residue (a dark orange gum) was purified by flash silica chromatography, elution gradient 0 to 40% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford methyl 2-chloro-4-methoxy-5-morpholinobenzoate (2.042 g, 80 %) as a pale yellow/cream crystalline solid.

Sources & evidence

ORD record
ord-bb0e774de3f94be78f90a0c79c7e9a7e
Source dataset
750 AstraZeneca ELN dataset
Original link
View source

Reaction notes

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