Potassium Hydroxide → Ammonia

HRID 37677Notes

Reaction equation

HRID 37677 reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:21]([O:23]C)=O)=[C:6]2[C:11]=1[O:10][CH2:9][C@H:8]([N:12]([CH:16]([CH2:19][CH3:20])[CH2:17][CH3:18])[CH2:13][CH2:14][CH3:15])[CH2:7]2.[OH-].[K+].O=S(Cl)Cl.FC1C=CC(C(O)=O)=C2C=1OC[C@H]([N:42](C(CC)CC)CCC)C2>CO.O.C(Cl)Cl.CN(C=O)C>[NH3:12].[C:21]([C:5]1[CH:4]=[CH:3][C:2]([F:1])=[C:11]2[C:6]=1[CH2:7][C@@H:8]([N:12]([CH:16]([CH2:19][CH3:20])[CH2:17][CH3:18])[CH2:13][CH2:14][CH3:15])[CH2:9][O:10]2)(=[O:23])[NH2:42]

Participants

10

Reactant 4

HCID 14797Potassium HydroxideHCID 24386Thionyl ChlorideHCID 53656554(R)-8-fluoro-5-carboxy-3-(N-3-pentyl-N-n-propylamino)chromanHCID 53912065(R)-8-Fluoro-5-methoxycarbonyl-3-(N-3-pentyl-N-n-propylamino)chroman

Product 2

HCID 222AmmoniaHCID 22853658(R)-5-Carbamoyl-8-Fluoro-3-(N-3-pentyl-N-n-propylamino)chroman

Reagents, catalysts & solvents 4

HCID 6228DimethylformamideCatalystHCID 887MethanolSolventHCID 962WaterSolventHCID 6344DichloromethaneSolvent

Procedure

(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.

Workup

  1. customgave
  2. customafter evaporation, and co-evaporation with toluene, (R)-8-fluoro-5-carboxy-3-(N-3-pentyl-N-n-propylamino)chroman as a white solid
  3. temperatureAfter reflux for 2 hours
  4. customthe slurry was evaporated
  5. dissolutionthe residue, dissolved in 10 ml dry THF
  6. additionwas added dropwise to 35 ml ice-
  7. temperaturecooled conc. NH3
  8. customThe THF was evaporated after 2 hours
  9. extractionextraction with EtOAc×2
  10. customdrying
  11. custom(Na2SO4) and evaporation
  12. customgave 0.51 g of a crude product
  13. customPurification by flash chromatography with hexane

Sources & evidence

ORD record
ord-96c80c4254034d32afcfc8658123dc09
Source dataset
uspto-grants-1995_05
Patent number
US05420151

Reaction notes

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