Реакция #65955

Уравнение реакции

(R)-8-Fluoro-5-methyloxycarbonyl-3-(N-3-pentyl-N-n-propylamino)chroman

KOH

SOCl2

(R)-8-fluoro-5-carboxy-3-(N-3-pentyl-N-n-propylamino)chroman

→

NH3

(R)-5-carbamoyl-8-fluoro-3-(N-3-pentyl-N-n-propylamino)chroman

Растворители

MeOH

H2O

CH2Cl2

Условия реакции

Обработка

1. 1
   Другоеgave
2. 2
   Другоеafter evaporation, and co-evaporation with toluene, (R)-8-fluoro-5-carboxy-3-(N-3-pentyl-N-n-propylamino)chroman as a white solid
3. 3
   ТемператураAfter reflux for 2 hours
4. 4
   Другоеthe slurry was evaporated
5. 5
   workup.DISSOLUTIONthe residue, dissolved in 10 ml dry THF
6. 6
   workup.ADDITIONwas added dropwise to 35 ml ice-
7. 7
   Температураcooled conc. NH3
8. 8
   ДругоеThe THF was evaporated after 2 hours
9. 9
   Экстракцияextraction with EtOAc×2
10. 10
    Другоеdrying
11. 11
    Другое(Na2SO4) and evaporation
12. 12
    Другоеgave 0.51 g of a crude product
13. 13
    ДругоеPurification by flash chromatography with hexane

Методика

(R)-8-Fluoro-5-methyloxycarbonyl-3-(N-3-pentyl-N-n-propylamino)chroman (0.72 g, 2.13 mmol) was hydrolysed with KOH (0.20 g, 3.1 mmol) in 20 ml MeOH and 10 ml H2O , under reflux conditions for 20 hours and gave after evaporation, and co-evaporation with toluene, (R)-8-fluoro-5-carboxy-3-(N-3-pentyl-N-n-propylamino)chroman as a white solid. SOCl2 (0.8 ml, 11 mmol) was added to a slurry of (R)-8-fluoro-5-carboxy-3-(N-3-pentyl-N-n-propylamino)chroman in 50 ml dry CH2Cl2 and 1 drop DMF (catalytic amount). After reflux for 2 hours, the slurry was evaporated, and the residue, dissolved in 10 ml dry THF was added dropwise to 35 ml ice-cooled conc. NH3 under stirring. The THF was evaporated after 2 hours and extraction with EtOAc×2, drying (Na2SO4) and evaporation gave 0.51 g of a crude product. Purification by flash chromatography with hexane:EtOAc:NH3, (60:40:0.5) gave 0.41 g of (R)-5-carbamoyl-8-fluoro-3-(N-3-pentyl-N-n-propylamino)chroman as light yellow crystals.

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