Benzenesulfonamide, 4-amino-N-[2-(4-morpholinyl)ethyl]- → 4-[4-(2,6-Dimethylpyridin-3-yloxy)pyridin-2-ylamino]-N-(2-morpholinoethyl)benzenesulfonamide

HRID 469

Reaction equation

HRID 469 reaction equation
Cc1ccc(Oc2ccnc(Cl)c2)c(C)n1.Nc1ccc(S(=O)(=O)NCCN2CCOCC2)cc1>CC(=O)N(C)C.CC(=O)O.CC(=O)O.CC1(C)c2cccc(P(c3ccccc3)c3ccccc3)c2Oc2c(P(c3ccccc3)c3ccccc3)cccc21.O=C([O-])[O-].[Cs+].[Cs+].[Pd]>Cc1ccc(Oc2ccnc(Nc3ccc(S(=O)(=O)NCCN4CCOCC4)cc3)c2)c(C)n1

Participants

7

Conditions

Temperature
150 °C

Procedure

In a 10 mL microwave reactor 3-(2-chloropyridin-4-yloxy)-2,6-dimethylpyridine (100 mg, 0.43 mmol) and 4-amino-N-(2-morpholinoethyl)benzenesulfonamide (122 mg, 0.43 mmol) were dissolved in DMA (5 mL) to give a tan solution.To the resultant solution Cesium carbonate (0.068 mL, 0.85 mmol) was added and sparged with nitrogen for 1 minute. Then Palladium(II) acetate (6.70 mg, 0.03 mmol) and 9,9-Dimethyl-4,5-bis(diphenylphosphino)xanthene (29.6 mg, 0.05 mmol) were added and the reaction mixture was sealed. The reaction was heated to150 °C for 25 minutes in the biotage microwave.The reaction was cooled to room temperature and LCMS shows reaction was completed. Reaction mixture was filtered through Celite Bed and washed with Dichloromethane. Filtrate was subjected to concentration to get DMA solution which was given to analytical department to purify using Mass based HPLC. After purification compound was isolated to get pale yellow solid of 4-(4-(2,6-dimethylpyridin-3-yloxy)pyridin-2-ylamino)-N-(2-morpholinoethyl)benzenesulfonamide (125 mg, 60.7 %)

Sources & evidence

ORD record
ord-7897aa67f78748769844b414acdceeae
Source dataset
750 AstraZeneca ELN dataset
Original link
View source

Linked notes

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