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
5-amino-3-((3-chlorophenyl)amino)-1H-pyrazole-4-carboxamide (100 mg) was then suspended in EtOH (4 mL) and 4,5,6,7-tetrafluoro-1H-indole-3-carbaldehyde (1 eq.) and piperidine (1 drop) were added. Stirred at reflux until intermediate was absent (HPLC). After reaction was complete (18 hrs) it was brought to room temperature and filtered to obtain product as a yellow powder. Powder was washed with EtOH. Product was allowed to dry under vacuum for 1 hr. Resulting imine was suspended in 5 mL MeOH and sodium borohydride (3 eq.) was added. HPLC confirmed reaction was complete (absence of imine). After completion (1 hr), precipitate was filtered to obtain D22 as a light yellow powder as product. Product was washed with deionized water to remove excess sodium borohydride.
WORKUP
后处理
- temperatureat reflux until intermediate
- customAfter reaction
- custom(18 hrs) it
- customwas brought to room temperature
- filtrationfiltered
- customto obtain product as a yellow powder
- washPowder was washed with EtOH
- customto dry under vacuum for 1 hr
- customreaction
- filtrationAfter completion (1 hr), precipitate was filtered
- customto obtain D22 as a light yellow powder as product
- washProduct was washed with deionized water
- customto remove excess sodium borohydride