反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a suspension of 2-{4-[8-fluoro-2-(2-isopropyl-5-methyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-1,3a-diazabenzo[e]azulen-9-ylsulfanyl]piperidin-1-yl}-2-methylpropionic acid (174 mg, 0.329 mmol) in DMF (5 mL) were added DIPEA (169 l, 0.987 mmol), HOBt.NH3 (75 mg, 0.494 mmol) and EDCI (95 mg, 0.494 mmol) and the reaction mixture was stirred at RT for 18 h. The mixture was then partitioned between EtOAc and water and the aqueous phase was further extracted with EtOAc (×3). The combined organic layers were washed with water, followed by brine, then dried and concentrated in vacuo. The resulting residue was purified by column chromatography (Si-PCC, gradient 3-15% MeOH in DCM) affording the title compound as a colorless sticky solid (96 mg, 56%). LCMS: RT 2.16 min [M+H]+ 527.8
WORKUP
后处理
- customThe mixture was then partitioned between EtOAc and water
- extractionthe aqueous phase was further extracted with EtOAc (×3)
- washThe combined organic layers were washed with water
- customdried
- concentrationconcentrated in vacuo
- customThe resulting residue was purified by column chromatography (Si-PCC, gradient 3-15% MeOH in DCM)