Dimethylformamide → HCID 86614656, compound

A mixture of 2-[4-(3-bromophenyl)-7-chloro-6-methyl-2-oxo-2H-chromen-3-yl]-N-[4-fluoro-2-(trifluoromethyl)phenyl]acetamide (2.00 g), palladium acetate (0.0079 g) and tri-o-tolyl phosphine (0.0214 g) was placed in a reaction vessel, and nitrogen was passed through the reaction vessel for 10 minutes to replace the atmosphere of the reaction vessel with nitrogen. N,N-Dimethylformamide (10 ml), butyl acrylate (0.677 g) and sodium acetate (0.317 g) were added successively thereto, and the mixture was stirred at room temperature for about 20 minutes. Then, the mixture was stirred at 110° C. for 3 hours and cooled to room temperature. Ethyl acetate (20 ml) and water (20 ml) were poured to the reaction mixture and, after stirring, an organic layer was separated. The organic layer was washed successively with a mixture of 10% saline (18 ml) and conc. hydrochloric acid (2 ml), and 10% saline (20 ml). Activated charcoal (0.1 g) and tributyl phosphine (0.0712 g) were added to the organic layer, and the mixture was stirred at room temperature for 10 minutes. Then, the activated charcoal was removed by filtration and washed with ethyl acetate (4 ml). The combined filtrate and washings were concentrated to 6.0 g under reduced pressure, and n-heptane (12 ml) was added dropwise to the residue to precipitate crystals. After stirring at 5° C. for 1 hour, the crystals were collected by filtration and washed with cold ethyl acetate/n-heptane (1/3, 4 ml). A mixture of the resulting crystals (2.06 g) and acetone (10 ml) were heated to 50° C. to dissolve the mixture, activated charcoal (0.1 g) was added thereto, and the mixture was stirred for 10 minutes. The activated charcoal was removed by filtration, and washed with acetone (4 ml). Water (4.6 ml) was added dropwise to the combined filtrate and washings, and the mixture was stirred at 5° C. for 1 hour. Crystals were collected by filtration, and washed with cold acetone/water (2/1, 4 ml) to obtain the title compound (1.84 g, yield 84.9%).

1. customwas placed in a reaction vessel
2. stirringThen, the mixture was stirred at 110° C. for 3 hours
3. temperaturecooled to room temperature
4. stirringafter stirring
5. customan organic layer was separated
6. washThe organic layer was washed successively with a mixture of 10% saline (18 ml) and conc. hydrochloric acid (2 ml), and 10% saline (20 ml)
7. additionActivated charcoal (0.1 g) and tributyl phosphine (0.0712 g) were added to the organic layer
8. stirringthe mixture was stirred at room temperature for 10 minutes
9. customThen, the activated charcoal was removed by filtration
10. washwashed with ethyl acetate (4 ml)
11. concentrationThe combined filtrate and washings were concentrated to 6.0 g under reduced pressure, and n-heptane (12 ml)
12. additionwas added dropwise to the residue
13. customto precipitate crystals
14. stirringAfter stirring at 5° C. for 1 hour
15. filtrationthe crystals were collected by filtration
16. washwashed with cold ethyl acetate/n-heptane (1/3, 4 ml)
17. additionA mixture of the resulting crystals (2.06 g) and acetone (10 ml)
18. temperaturewere heated to 50° C.
19. dissolutionto dissolve the mixture, activated charcoal (0.1 g)
20. additionwas added
21. stirringthe mixture was stirred for 10 minutes
22. customThe activated charcoal was removed by filtration
23. washwashed with acetone (4 ml)
24. additionWater (4.6 ml) was added dropwise to the combined filtrate and washings
25. stirringthe mixture was stirred at 5° C. for 1 hour
26. filtrationCrystals were collected by filtration
27. washwashed with cold acetone/water (2/1, 4 ml)

ORD record

ord-9113f16d1a0442b68ed140c72bcd2d32

Source dataset

uspto-grants-2009_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07541478B2