反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
CONDITIONS
反应条件
- 温度
- 100 °C
PROCEDURE
实验过程
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]+.
WORKUP
后处理
- temperaturethe reaction cooled
- concentrationThe reaction mixture was concentrated
- additionThe reaction mixture wad diluted with CH2Cl2 (300 mL) and water (300 mL)
- extractionThe mixture was extracted with 1% MeOH in CH2Cl2 (4×)
- dry with materialThe CH2Cl2 layer were dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated to 400 mL
- additionEthanol (400 mL) was added to the reaction mixture
- concentrationconcentrated to dryness
- additionEthanol (400 mL) was added again to the reaction mixture
- concentrationconcentrated to dryness
- additionEthanol (500 mL) was added to the reaction mixture
- temperaturerefluxed
- waitAfter 4 h
- temperaturethe reaction mixture was cooled to 0° C.
- filtrationfiltered
- washwash with EtOH
- customThe product was dried under vacuum at 60° C. for 2 days