反应详情

To tetrahydrofuran (50 ml) are added 4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyric acid (45 mmole) and pyridine (50 mmole), and thereto is added dropwide with stirring methyl bromoformate (50 mmole) with keeping the inner temperature at 5°-15° C. by ice-cooling, and thereafter, the mixture is stirred at room temperature for one hour. To the mixture is added 4-methylcyclohexylamine (55 mmole), and the mixture is further stirred for 3 hours. After the reaction, the solvent is distilled off under reduced pressure, and the residue is dissolved in chloroform. The chloroform layer is washed with dilute aqueous sodium hydroxide solution, diluted hydrochloric acid and water in order, and dried over sodium sulfate. Inorganic materials are filtered off and the mother liquor is concentrated. The resulting residue is subjected to column chromatography (Wakogel C-200, eluting solvent, benzene:chloroform=4:1, V/V) to isolate N-(4-methylcyclohexyl)-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide (yield: 45%).

1. customat 5°-15° C.
2. temperaturecooling
3. stirringthe mixture is further stirred for 3 hours
4. customAfter the reaction
5. distillationthe solvent is distilled off under reduced pressure
6. dissolutionthe residue is dissolved in chloroform
7. washThe chloroform layer is washed with dilute aqueous sodium hydroxide solution, diluted hydrochloric acid and water in order
8. dry with materialdried over sodium sulfate
9. filtrationInorganic materials are filtered off
10. concentrationthe mother liquor is concentrated
11. washThe resulting residue is subjected to column chromatography (Wakogel C-200, eluting solvent, benzene:chloroform=4:1, V/V)