反应详情

A mixture of 40 parts of 1-[(2,4-difluorophenyl)thioxomethyl]-4-(phenylmethyl)piperazine, 144 parts of 1-butanol, 13 parts of hydrazine monohydrate and 24 parts of acetic acid was stirred overnight at reflux temperature. After cooling, 50 parts of sodium carbonate were added and stirring was continued for 3 hours at reflux temperature. The reaction mixture was cooled until room temperature and water and methylbenzene were added. After stirring for 15 minutes, the separated organic layer was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (92:8 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 12 parts (32.2%) of 6-fluoro-3-[4-(phenylmethyl)piperazinyl]-1H-indazole; mp. 162.0° C. (int. 7).

1. temperatureat reflux temperature
2. temperatureAfter cooling
3. stirringstirring
4. waitwas continued for 3 hours
5. temperatureat reflux temperature
6. stirringAfter stirring for 15 minutes
7. customthe separated organic layer was dried
8. filtrationfiltered
9. customevaporated
10. customThe residue was purified by column chromatography over silica gel using
11. additiona mixture of trichloromethane and methanol (92:8 by volume) as eluent
12. customThe pure fractions were collected
13. customthe eluent was evaporated
14. customThe residue was crystallized from acetonitrile
15. filtrationThe product was filtered off
16. customdried