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

HRID 581Notes

Reaction equation

HRID 581 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 (9.9 g, 50.25 mmol), morpholine (7.96 mL, 100.49 mmol), sodium 2-methylpropan-2-olate (19.32 g, 200.98 mmol),dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphine (2.345 g, 5.02 mmol) in degassed dioxane (200 mL) was added diacetoxypalladium (0.564 g, 2.51 mmol) and the reaction mixture was heated under nitrogen at 90 °C for 17 hours, then evaporated and partitioned between DCM (150 mL) and saturated aqueous sodium bicarbonate solution (150 mL). The aqueous phase was extracted further with DCM (70 mL) and the combined organics were concentrated. The crude material was purified by flash silica chromatography, elution gradient 0 to 5% MeOH in DCM. Pure fractions were evaporated to dryness to afford 4-(1H-pyrrolo[2,3-b]pyridin-5-yl)morpholine (9.28 g, 91 %) as a yellow solid.

Sources & evidence

ORD record
ord-d96d0e3f2950466bac2ca8525ac77415
Source dataset
750 AstraZeneca ELN dataset
Original link
View source

Reaction notes

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