HCID 15338089, compound → HCID 23355438, compound

HRID 1720948Notes

Reaction equation

HRID 1720948 reaction equation
[CH:1]1([N:6]2[C:10]3[C:11](=O)[N:12]([C:14]4[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=4)[CH2:13][C:9]=3[C:8]([CH2:21][CH3:22])=[N:7]2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>CCOCC>[CH:1]1([N:6]2[C:10]3[CH2:11][N:12]([C:14]4[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=4)[CH2:13][C:9]=3[C:8]([CH2:21][CH3:22])=[N:7]2)[CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

4

Conditions

Temperature
0 °C

Procedure

To a stirred solution of 1-cyclopentyl-3-ethyl-6-oxo-5-phenyl-4,6-dihydro-1H-pyrazolo[3,4-c]pyrrole (0.17 g, 0.58 mmole) in anhydrous ether (15 ml) was added lithium aluminum hydride (0.17 g, 4.6 mmole). The majority of the ether (12-13 ml) was then removed by distillation, and the remaining mixture diluted with toluene (25 ml) and heated to reflux over 24 hours. The mixture was cooled to 0° C. and cautiously treated with ice. The resulting mixture was filtered through celite, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude residue was chromatographed on a silica column using 1:9 ethyl acetate/hexane as eluent to give 100 mg of a colorless oil. 1H NMR (250 MHz, CDCl3) δ 1.26 (t, J=7.6 Hz, 3H), 1.65-2.25 (m, 8H), 2.67 (q, J=7.6 Hz, 2H), 4.35 (s, 2H), 4.45 (s, 2H), 4.53 (pentet, J=7.5 Hz, 1H), 6.61 (d, J=8.1 Hz, 2H), 6.74 (t, J=7.4 Hz, 1H), 7.29 (dd, J=7.5 and 8.4 Hz, 2H); MS m/z 282.

Workup

  1. customThe majority of the ether (12-13 ml) was then removed by distillation
  2. additionthe remaining mixture diluted with toluene (25 ml)
  3. temperatureheated
  4. temperatureto reflux over 24 hours
  5. additioncautiously treated with ice
  6. filtrationThe resulting mixture was filtered through celite
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe crude residue was chromatographed on a silica column

Sources & evidence

ORD record
ord-1e0cc65b10cf49b085e6c419234fad76
Source dataset
uspto-grants-1996_04
Patent number
US05508300

Reaction notes

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