Water → HCID 20437853, compound

HRID 1759623Notes

Reaction equation

HRID 1759623 reaction equation
[H-].[Na+].[O:3]=[C:4]1[NH:9][CH2:8][CH2:7][N:6]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH:5]1[CH:17]([OH:25])[C:18]1[CH:23]=[CH:22][C:21]([F:24])=[CH:20][CH:19]=1.[CH3:26][O:27][CH2:28][CH2:29][O:30][CH2:31]Cl.O>CCCCCC.CN(C)C=O>[O:3]=[C:4]1[NH:9][CH2:8][CH2:7][N:6]([C:10]([O:12][C:13]([CH3:16])([CH3:14])[CH3:15])=[O:11])[CH:5]1[CH:17]([O:25][CH2:26][O:27][CH2:28][CH2:29][O:30][CH3:31])[C:18]1[CH:19]=[CH:20][C:21]([F:24])=[CH:22][CH:23]=1

Participants

7

Conditions

Temperature
0 °C

Procedure

To 0.13 g (0.0054 mole) of NaH (0.22 g of a 61% dispersion in oil, washed with hexane) in 10 ml of dimethylformamide (DMF) was added 1.6 g of 35 in 20 ml of dry DMF, and the mixture stirred at 0° C. for 30 minutes. A solution of 0.67 g (0.0055 mole) of (2-methoxyethoxy)methyl chloride in 5 ml of dry DMF was added and the mixture allowed to warm to room temperature, stirred for 1 hour, and poured into 50 ml of water. The product was extracted into ethyl acetate and the extract washed with brine and dried over MgSO4. After filtration, the solvent was removed at reduced pressure and the residue triturated with hexane and filtered to give the title compound.

Workup

  1. temperatureto warm to room temperature
  2. stirringstirred for 1 hour
  3. extractionThe product was extracted into ethyl acetate
  4. washthe extract washed with brine
  5. dry with materialdried over MgSO4
  6. filtrationAfter filtration
  7. customthe solvent was removed at reduced pressure
  8. customthe residue triturated with hexane
  9. filtrationfiltered

Sources & evidence

ORD record
ord-fe4e519f51ba4514930fd677c254b63c
Source dataset
uspto-grants-1982_07
Patent number
US04341698

Reaction notes

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