反应详情

200 mg of 6-(3-phenylamino-4-aminophenyl)oxyhexanoic acid methyl ester was dissolved in 2 ml of methanol, the solution was mixed with 90 μl of propylisothiocyanate, and the mixture was heated for 3 hours to 50° C. After cooling, it was mixed with saturated ammonium chloride solution, diluted with water, extracted three times with ethyl acetate, the combined organic phases were washed with saturated sodium chloride solution, dried on sodium sulfate and concentrated by evaporation in a vacuum. The residue was purified by column chromatography on silica gel. 140 mg of a thiourea derivative, which was dissolved in 1.5 ml of methanol, was obtained. 0.16 ml of iodomethane was added to this solution, and it was refluxed for 4 hours. After cooling, it was mixed with 1N aqueous hydrochloric acid, extracted three times with ethyl acetate, the combined organic phases were washed with saturated sodium chloride solution, dried on sodium sulfate and concentrated by evaporation in a vacuum. The residue was purified by column chromatography on silica gel. 72 mg was obtained.

1. temperaturethe mixture was heated for 3 hours to 50° C
2. temperatureAfter cooling
3. extractionextracted three times with ethyl acetate
4. washthe combined organic phases were washed with saturated sodium chloride solution
5. customdried on sodium sulfate
6. concentrationconcentrated by evaporation in a vacuum
7. customThe residue was purified by column chromatography on silica gel
8. dissolution140 mg of a thiourea derivative, which was dissolved in 1.5 ml of methanol
9. customwas obtained
10. temperaturewas refluxed for 4 hours
11. temperatureAfter cooling
12. extractionextracted three times with ethyl acetate
13. washthe combined organic phases were washed with saturated sodium chloride solution
14. customdried on sodium sulfate
15. concentrationconcentrated by evaporation in a vacuum
16. customThe residue was purified by column chromatography on silica gel
17. custom72 mg was obtained