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
0.882 mL (10.07 mmol) of oxalyl chloride was added dropwise to a solution of 2-(3-methylsulfanyl-propionylamino)-3-phenyl-propionic acid methyl ester (from previous step) in 30 mL of dichloromethane and stirred at room temperature for 1 h. This reaction mixture was then cooled to −10° C. and treated with 1.82 g (11 mmol) of FeCl3 at this temperature in portions. This reaction mixture was allowed to warm up to room temperature overnight. 30 mL of 2 N aq. HCl was added slowly while stirring for 1 h. 20 mL of dichloromethane was added and separated, washed again with water (50 mL), and dried over sodium sulfate. The organic solvents were evaporated in vacuo. The residual red solid was mixed with 30 mL of methanol and 1.5 mL of conc. H2SO4 and heated under reflux overnight. Water was added to the reaction mixture and the methanol was evaporated under reduced pressure. Ammonium hydroxide was added to adjust pH to basic. The aqueous layer (˜50 mL) was extracted with dichloromethane (2×50 mL). The combined organic layers were dried over sodium sulfate and evaporated. Purification by column chromatography on silica gel gave 923 mg (38%) of 1-(2-methylsulfanyl-ethyl)-3,4-dihydro-isoquinoline-3-carboxylic acid methyl ester. LCMS: 264 (M+1)+.
WORKUP
后处理
- temperatureThis reaction mixture was then cooled to −10° C.
- temperatureto warm up to room temperature overnight
- stirringwhile stirring for 1 h
- customseparated
- washwashed again with water (50 mL)
- dry with materialdried over sodium sulfate
- customThe organic solvents were evaporated in vacuo
- additionThe residual red solid was mixed with 30 mL of methanol and 1.5 mL of conc. H2SO4
- temperatureheated
- temperatureunder reflux overnight
- additionWater was added to the reaction mixture
- customthe methanol was evaporated under reduced pressure
- additionAmmonium hydroxide was added
- extractionThe aqueous layer (˜50 mL) was extracted with dichloromethane (2×50 mL)
- dry with materialThe combined organic layers were dried over sodium sulfate
- customevaporated
- customPurification by column chromatography on silica gel