反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 85 °C
PROCEDURE
实验过程
To a mixture of 2-[N-(cyclopentylmethyl)-N-ethylamino]-6-methyl-5-nitronicotinonitrile (1.22 g, 4.23 mmol) in DMF (10 mL) is added N,N-dimethylformamide diethyl acetal (1.09 mL, 6.35 mmol). After stirring at 85° C. for 30 min, the reaction mixture is cooled to room temperature and then H2O is added. The mixture is extracted with EtOAc, dried over sodium sulfate and concentrated in vacuo. The resulting solid is rinsed with MeOH to give an orange solid. The solid is dissolved in MeOH (200 mL) and EtOAc (200 mL) and treated with Palladium-activated carbon ethylenediamine complex (Pd/C(en), 470 mg). The mixture is stirred under H2 atmosphere for 2.5 hours at room temperature. The reaction mixture is filtered, and the filtrate is concentrated in vacuo. The residue is dissolved in EtOAc/Hexane and passed through a silica-gel pad. The resulting mixture is concentrated in vacuo, and the residue is dissolved in DMF (10 mL). To this mixture, NaH (0.54 g, 13.5 mmol) is added at 0° C., and after 30 min, iodomethane (0.28 mL, 4.50 mmol) is added. After stirring for 1 hour, the reaction is quenched with H2O. The mixture is extracted with EtOAc and washed with brine. The organic layer is dried over sodium sulfate and concentrated in vacuo. The residue is purified by silica-gel column chromatography to give 5-[N-(cyclopentylmethyl)-N-ethylamino]-1-methyl-1H-pyrrolo[3,2-b]pyridine-6-carbonitrile as a colorless oil.
WORKUP
后处理
- temperaturethe reaction mixture is cooled to room temperature
- extractionThe mixture is extracted with EtOAc
- dry with materialdried over sodium sulfate
- concentrationconcentrated in vacuo
- washThe resulting solid is rinsed with MeOH
- customto give an orange solid
- stirringThe mixture is stirred under H2 atmosphere for 2.5 hours at room temperature
- filtrationThe reaction mixture is filtered
- concentrationthe filtrate is concentrated in vacuo
- dissolutionThe residue is dissolved in EtOAc/Hexane
- concentrationThe resulting mixture is concentrated in vacuo
- dissolutionthe residue is dissolved in DMF (10 mL)
- waitafter 30 min
- stirringAfter stirring for 1 hour
- customthe reaction is quenched with H2O
- extractionThe mixture is extracted with EtOAc
- washwashed with brine
- dry with materialThe organic layer is dried over sodium sulfate
- concentrationconcentrated in vacuo
- customThe residue is purified by silica-gel column chromatography