Morpholine → 5-(Morpholin-4-yl)-1H-pyrrolo[2,3-b]pyridine

HRID 580Notes

Reaction equation

HRID 580 reaction equation
Brc1cnc2[nH]ccc2c1.C1COCCN1>C1COCCO1.CC(=O)O.CC(=O)O.CC(C)(C)[O-].CC(C)Oc1cccc(OC(C)C)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1.[Na+].[Pd]>c1cc2cc(N3CCOCC3)cnc2[nH]1

Participants

7

Conditions

Temperature
90 °C

Procedure

To a mixture of 5-bromo-1H-pyrrolo[2,3-b]pyridine (5.1 g, 25.88 mmol), morpholine (4.10 mL, 51.77 mmol), sodium 2-methylpropan-2-olate (9.95 g, 103.54 mmol),dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphine (0.604 g, 1.29 mmol) in degassed dioxane (100 mL) was added diacetoxypalladium (0.581 g, 2.59 mmol) and the reaction mixture was heated under nitrogen at 90 °C for 17 hours, then evaporated and partitioned between DCM (80ml) and saturated aqueous sodium bicarbonate solution (80ml). The aqueous phase was extracted further with DCM (50ml) and the combined organics were evaporated, redissolved in a mixture of methanol and DCM and purified by flash silica chromatography, elution gradient 0 to 10% MeOH in DCM. Pure fractions were evaporated to dryness to afford 4-(1H-pyrrolo[2,3-b]pyridin-5-yl)morpholine (3.40 g, 64.6 %) as a yellow solid.

Sources & evidence

ORD record
ord-c34fe67f0c724f1db0a5e6644d227638
Source dataset
750 AstraZeneca ELN dataset
Original link
View source

Reaction notes

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