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
CONDITIONS
反应条件
- 温度
- 100 °C
PROCEDURE
实验过程
A mixture of 4,6-dichloro-2-(2,4-dimethoxybenzyl)-7-fluoro-1H-pyrrolo[3,4-c]pyridin-3(2H)-one (4.8 g, 12.93 mmol) and tert-butyl (1S,2R)-2-aminocyclohexylcarbamate (4.16 g, 19.40 mmol) and diisopropylethylamine (3.39 mL, 19.40 mmol) in ACN (20 mL) was stirred at 100° C. for 3 days. Water and EtOAc were added and the aqueous phase was extracted with EtOAc. The organic phases were combined, washed with brine, dried over MgSO4, and evaporated. The residue was purified by chromatography on SiO2 (Hexane/EtOAc=1/1) to give the title compound as a brown amorphous solid (3.31 g, 46.6%). 1H NMR (500 MHz, CDCl3) δ ppm 1.35-2.02 (m, 17 H), 3.80 (s, 3 H), 3.84 (s, 3 H), 4.01 (br s, 1 H), 4.20 (s, 2H), 4.23 (br s, 1 H), 4.66 (s, 2 H), 4.91 (br s, 1 H), 6.40-6.52 (m, 2 H), 7.20-7.28 (m, 1 H). [M+H] calc'd for C27H34ClFN4O5, 549; found, 549.
WORKUP
后处理
- extractionthe aqueous phase was extracted with EtOAc
- washwashed with brine
- dry with materialdried over MgSO4
- customevaporated
- customThe residue was purified by chromatography on SiO2 (Hexane/EtOAc=1/1)