Ammonia hydroxide → N-{3-[5-(2-Amino-4-pyrimidinyl)-2-(tetrahydro-2H-pyran-4-yl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide

Temperature

100 °C

A suspension of N-{3-[5-(2-chloro-4-pyrimidinyl)-2-(tetrahydro-2H-pyran-4-yl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide (20.7 g, 36.5 mmol) and ammonia hydroxide (500 mL) was heated in a steel reactor to 100° C. After 3 h, the reaction cooled and checked by HPLC. The reaction mixture was concentrated. The reaction mixture wad diluted with CH2Cl2 (300 mL) and water (300 mL) then acidified with 6 N HCl to pH=1. The mixture was extracted with 1% MeOH in CH2Cl2 (4×). The CH2Cl2 layer were dried over Na2SO4 and filtered and concentrated to 400 mL. Ethanol (400 mL) was added to the reaction mixture and concentrated to dryness. Ethanol (400 mL) was added again to the reaction mixture and concentrated to dryness. Ethanol (500 mL) was added to the reaction mixture and refluxed. After 4 h, the reaction mixture was cooled to 0° C., filtered, and wash with EtOH. The product was dried under vacuum at 60° C. for 2 days. Title compound was obtained as an off-white solid (17 g, 85% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 10.90 (br. s., 1H), 7.98 (d, J=5.3 Hz, 1H), 7.56-7.84 (m, 1H), 6.93-7.54 (m, 5H), 6.77 (br. s., 2H), 5.85 (d, J=4.6 Hz, 1H), 3.92 (d, J=9.9 Hz, 2H), 3.46 (t, J=11.2 Hz, 2H), 3.20-3.32 (m, 1H), 1.90-2.06 (m, 2H), 1.57-1.81 (m, 2H). MS (ESI): 548.10 [M+H]+.

1. temperaturethe reaction cooled
2. concentrationThe reaction mixture was concentrated
3. additionThe reaction mixture wad diluted with CH2Cl2 (300 mL) and water (300 mL)
4. extractionThe mixture was extracted with 1% MeOH in CH2Cl2 (4×)
5. dry with materialThe CH2Cl2 layer were dried over Na2SO4
6. filtrationfiltered
7. concentrationconcentrated to 400 mL
8. additionEthanol (400 mL) was added to the reaction mixture
9. concentrationconcentrated to dryness
10. additionEthanol (400 mL) was added again to the reaction mixture
11. concentrationconcentrated to dryness
12. additionEthanol (500 mL) was added to the reaction mixture
13. temperaturerefluxed
14. waitAfter 4 h
15. temperaturethe reaction mixture was cooled to 0° C.
16. filtrationfiltered
17. washwash with EtOH
18. customThe product was dried under vacuum at 60° C. for 2 days

ORD record

ord-14f6259bc1254d4a93f22af0d00038ed

Source dataset

uspto-grants-2014_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08642759B2