Реакция #84239

Уравнение реакции

4-Fluoro-phenyl thiol

NaH

5-chloro-1-methanesulfonyl-2-(2-methyl-oxiranyl)-6-trifluoromethyl-1H-indole

→

title compound

2-(5-Chloro-6-trifluoromethyl-1H-indol-2-yl)-1-(4-fluoro-phenylsulfanyl)-propan-2-ol

Растворители

THF

THF

Условия реакции

Обработка

1. 1
   workup.ADDITIONwas added into the reaction via syringe
2. 2
   ДругоеTHF was removed
3. 3
   Другоеthe residue was partitioned between CH2Cl2 and water
4. 4
   ПромывкаThe organic layer was washed with brine
5. 5
   Сушкаdried over anhydrous Na2SO4
6. 6
   Концентрированиеconcentrated
7. 7
   Другоеto yield a crude white solid
8. 8
   ДругоеThe crude material was purified

Методика

4-Fluoro-phenyl thiol (55 mg, 0.425 mmoL) was treated with NaH (60%, 17 mg, 0.425 mmoL) in THF (2 mL) at 0° C. After 10 min., 5-chloro-1-methanesulfonyl-2-(2-methyl-oxiranyl)-6-trifluoromethyl-1H-indole, the epoxide derivative compound prepared as in Example 72 (100 mg, 0.425 mmoL) in THF (1 mL) was added into the reaction via syringe. The reaction was slowly warmed to room temperature. THF was removed and the residue was partitioned between CH2Cl2 and water. The organic layer was washed with brine and dried over anhydrous Na2SO4, then concentrated to yield a crude white solid. The crude material was purified using column chromatography (silica gel, 3:1 hexanes:EtOAc as eluent) to yield the title compound as a white solid.

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