Sodium hydride → HCID 67502225, compound

HRID 1625228Notes

Reaction equation

HRID 1625228 reaction equation
[H-].[Na+].[Cl:3][C:4]1[CH:9]=[CH:8][N:7]=[C:6]2[NH:10][CH:11]=[C:12]([CH2:13][CH3:14])[C:5]=12.Cl[CH2:16][O:17][CH2:18][CH2:19][Si:20]([CH3:23])([CH3:22])[CH3:21]>CN(C=O)C>[Cl:3][C:4]1[CH:9]=[CH:8][N:7]=[C:6]2[N:10]([CH2:16][O:17][CH2:18][CH2:19][Si:20]([CH3:23])([CH3:22])[CH3:21])[CH:11]=[C:12]([CH2:13][CH3:14])[C:5]=12

Participants

5

Procedure

Sodium hydride (0.877 g, a 55% dispersion in paraffin liquid) was added to a solution of compound (41c) (3.3 g) in DMF (61 mL) at 0° C., followed by stirring for 10 min. Then, [2-(chloromethoxy)ethyl]trimethylsilane (3.53 mL) was added to the reaction solution, followed by stirring at room temperature for 1 hr. After cooling, ice water was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated saline in this order and was then dried over anhydrous sodium sulfate. After distillation of the solvent, the residue was purified by neutral silica gel column chromatography (n-hexane/ethyl acetate) to obtain compound (41d) (4.30 g, 76%) as a colorless oily substance.

Workup

  1. stirringby stirring at room temperature for 1 hr
  2. temperatureAfter cooling
  3. extractionfollowed by extraction with ethyl acetate
  4. washThe organic layer was washed with water and saturated saline in this order
  5. dry with materialwas then dried over anhydrous sodium sulfate
  6. distillationAfter distillation of the solvent
  7. customthe residue was purified by neutral silica gel column chromatography (n-hexane/ethyl acetate)

Sources & evidence

ORD record
ord-224fc7b33ac847578e968ff8a41fbdc9
Source dataset
uspto-grants-2014_07
Patent number
US08779142B2

Reaction notes

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