反应详情
EQUATION
反应方程式
REACTANTS
反应物
Sodium Bicarbonate
CHNaO3
3-(2-Quinolinyl)acrylic acid
C12H9NO2
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride
C8H18ClN3
1H-Benzotriazol-1-ol--water (1/1)
C6H7N3O2
N-[3-(6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenyl)methanesulfonamide
C13H18N2O2S
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A solution of 1-hydroxybenzotriazole monohydrate (112 mg, 0.73 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (153 mg, 0.80 mmol) in N,N-dimethylformamide (5 ml) was added to (E)-3-(2-quinolinyl)-2-propenoic acid (M. Hamana, K. Funakoshi and Y. Kuchino, Chem. Pharm. Bull., 1974, 22, 1806; 131 mg, 0.66 mmol). After stirring at room temperature for 15 min, the mixture was added to the hydrochloride salt of N-[3-(6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenyl]methanesulfonamide (Preparation 53, 202 mg, 0.66 mmol) and sodium hydrogen carbonate (110 mg, 1.32 mmol). The reaction mixture was stirred at room temperature for overnight and then water (10 ml) and dichloromethane (5 ml) were added. The biphasic mixture was separated by filtering through a Whatman Microfiltration Device Filter Tube, and the resulting organic extract was concentrated using a stream of nitrogen to afford 400 mg of a crude dark red oil. This was purified by chromatography using a Biotage Flash 40S™ cartridge packed with silica gel (40 g) eluting with dichloromethane:ethanol: 0.880 ammonia (100:2 1) to afford the title compound as a cream solid (206 mg, 70%).
WORKUP
后处理
- stirringThe reaction mixture was stirred at room temperature for overnight
- customThe biphasic mixture was separated
- filtrationby filtering through a Whatman Microfiltration Device
- filtrationFilter Tube
- extractionthe resulting organic extract
- concentrationwas concentrated
- customto afford 400 mg of a crude dark red oil
- customThis was purified by chromatography
- washeluting with dichloromethane