Dimethylformamide → HCID 66929778, compound

HRID 398298Notes

Reaction equation

HRID 398298 reaction equation
[NH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.CN([CH:10]=[O:11])C>>[NH2:1][C@@H:6]([CH:5]1[CH2:6][C:5]2[C:3](=[CH:2][CH:2]=[CH:3][CH:4]=2)[CH2:4]1)[CH2:10][OH:11]

Participants

3

Conditions

Temperature
25 °C

Procedure

20% Piperidine in DMF (15 mL) was added to a solution of 9 H-fluoren-9-ylmethyl-(1S)-1-(2,3-dihydro-1H-inden-2-yl)-2-hydroxyethylcarbamate (1.05 g, 2.63 mmol) in DMF (5 mL). The reaction was stirred at 25° C. for 19 h. After solvent evaporation, the crude product was dissolved in ethyl acetate (50 mL) and dried over MgSO4, filtered and concentrated to obtain a crude yellow oil (1.05 g). Mass Spectrum (+ESI): 179 (M+H)+.

Workup

  1. customAfter solvent evaporation
  2. dissolutionthe crude product was dissolved in ethyl acetate (50 mL)
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-1ffdbe62e7554277833aabc06b28eb4f
Source dataset
uspto-grants-2003_08
Patent number
US06610734B2

Reaction notes

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