Potassium Carbonate → N-{3-[2,6-dichloro-4-(3,5-dimethyl-1,2-oxazol-4-yl)benzoyl]-1H-pyrrolo[2,3-c]pyridin-7-yl}cyclopropanecarboxamide

温度

90 °C

A mixture of N-[3-(4-bromo-2,6-dichlorobenzoyl)-1H-pyrrolo[2,3-c]pyridin-7-yl]cyclopropanecarboxamide (0.1 g, 0.2 mmol) and (3,5-dimethyl-1,2-oxazol-4-yl)boronic acid (0.037 g, 0.26 mmol) was taken in a vial. To the reaction mixture, 1,4 dioxane (3 mL), potassium carbonate (0.091 g, 0.6 mmol) and water (0.5 mL) were added. The whole reaction mixture was stirred with argon gas for about five minutes. Finally dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) (0.018 g, 0.02 mmol) was added to the reaction mixture, the vial was sealed properly and heated at 90° C. for about 4 hours. The reaction mixture was cooled to room temperature, followed by addition of water (25 mL), extracted with ethyl acetate (2×50 mL). The organic layer was dried over anhydrous sodium sulphate and concentrated under vacuum to get the crude. The crude was purified by preparative thin layer chloromatography using methanol (6%) in dicloromethane to obtain N-{3-[2,6-dichloro-4-(3,5-dimethyl-1,2-oxazol-4-yl)benzoyl]-1H-pyrrolo[2,3-c]pyridin-7-yl}cyclopropanecarboxamide (0.015 g, 15%).

1. customThe whole reaction mixture
2. customthe vial was sealed properly
3. temperatureThe reaction mixture was cooled to room temperature
4. extractionextracted with ethyl acetate (2×50 mL)
5. dry with materialThe organic layer was dried over anhydrous sodium sulphate
6. concentrationconcentrated under vacuum
7. customto get the crude
8. customThe crude was purified by preparative thin layer chloromatography

ORDレコード

ord-51e809406e0f4dc58c7d5f5ee32634a8

出典データセット

uspto-grants-2016_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09364466B2