6-Methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamine → 2-(3,3-Difluorocyclobutyl)-N-(6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)-4-methyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine
Reaction equation
CN1Cc2ccc(Cl)nc2OC(C2CC(F)(F)C2)C1.COc1nc(N)ccc1-c1cnn(C)c1>C1COCCO1.CC(=O)O.CC(=O)O.CC1(C)c2cccc(P(c3ccccc3)c3ccccc3)c2Oc2c(P(c3ccccc3)c3ccccc3)cccc21.O=C([O-])[O-].[Cs+].[Cs+].[Pd]>COc1nc(Nc2ccc3c(n2)OC(C2CC(F)(F)C2)CN(C)C3)ccc1-c1cnn(C)c1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 4
Conditions
- Temperature
- 145 °C
Procedure
Palladium(II) acetate (0.019 g, 0.08 mmol) and 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene (0.096 g, 0.17 mmol) were added to a degassed solution of 8-chloro-2-(3,3-difluorocyclobutyl)-4-methyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepine (0.160 g, 0.55 mmol), 6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-amine (0.113 g, 0.55 mmol) and Cesium carbonate (0.058 mL, 0.72 mmol) in dry dioxane (15 mL). The reaction was heated in a microwave oven at 145°C for 1h. About 50% of product. The reaction was heated at 145°C for another 30 min. About 45% of product. The reaction was interrupted and the reaction mixture was pooled with the corresponding mixture in EN04426-52. The reaction mixture was filtered through a plug of celite. The celite was washed with DCM. The solvents were evaporated and the crude was purified by ISCO on a 25 g column with an increased gradient of DCM/MeOH (90/10) 0-50% in DCM) to give 0.176 g (35%) of the product. The enatiomers were also separated (see EN04426-56).
Sources & evidence
- ORD record
- ord-bf7cf9ac04cd4fedb1f93e4a263e0d2f
- Source dataset
- 750 AstraZeneca ELN dataset
- Original link
- View source
Reaction notes
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