Morpholine → HCID 57422999, compound

HRID 417Notes

Reaction equation

HRID 417 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

Methyl 5-bromo-2-chloro-4-methoxybenzoate (1.486 g, 5.32 mmol), 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.132 g, 0.21 mmol), palladium(II) acetate (0.024 g, 0.11 mmol) and cesium carbonate (2.425 g, 7.44 mmol) were mixed together and evacuated then purged with nitrogen. Toluene (10 mL) and morpholine (0.464 mL, 5.32 mmol) were added and the mixture evacuated and purged with nitrogen several times. The suspension (red) was heated to 100 °C for 18 hours under nitrogen. The mixture was allowed to cool to ambient temperature and filtered, washing with EtOAc. The filtrate was concentrated to provide an orange residue. The crude product was purified by flash silica chromatography, elution gradient 0 to 35% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford methyl 2-chloro-4-methoxy-5-morpholinobenzoate (0.826 g, 54.4 %) as a cream crystalline solid. Lower than expected yield (previously recorded 80% EN04398-06).....not sure what has happened.

Sources & evidence

ORD record
ord-ae9e42c4adac4ee7b754752b65453944
Source dataset
750 AstraZeneca ELN dataset
Original link
View source

Reaction notes

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