Imidazole → HCID 15093123, compound

HRID 1463899Notes

Reaction equation

HRID 1463899 reaction equation
Cl[CH2:2][C:3]([NH:5][CH:6]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[CH2:10][O:9][C:8]2[CH:17]=[CH:18][C:19]([C:21]([O:23][CH3:24])=[O:22])=[CH:20][C:7]1=2)=[O:4].[NH:25]1[CH:29]=[CH:28][N:27]=[CH:26]1>C1(C)C=CC=CC=1>[N:25]1([CH2:2][C:3]([NH:5][CH:6]2[C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=3[CH2:10][O:9][C:8]3[CH:17]=[CH:18][C:19]([C:21]([O:23][CH3:24])=[O:22])=[CH:20][C:7]2=3)=[O:4])[CH:29]=[CH:28][N:27]=[CH:26]1

Participants

4

Procedure

Crude methyl 11-chloroacetamido-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate, 3.0 g, was heated to reflux for 4 hours in 100 ml of toluene together with 0.9 g of imidazole. After allowing to cool, the solvent was distilled off under reduced pressure. The obtained residue was extracted with 300 ml of methylene chloride. The extract was washed successively with saturated sodium bicarbonate aqueous solution and saturated sodium chloride aqueous solution. After drying over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was subjected to silica gel column chromatography .(eluting solvent; chloroform:methanol=10:1) to give 1.6 g of the product.

Workup

  1. temperatureto cool
  2. distillationthe solvent was distilled off under reduced pressure
  3. extractionThe obtained residue was extracted with 300 ml of methylene chloride
  4. washThe extract was washed successively with saturated sodium bicarbonate aqueous solution and saturated sodium chloride aqueous solution
  5. dry with materialAfter drying over anhydrous sodium sulfate
  6. distillationthe solvent was distilled off under reduced pressure

Sources & evidence

ORD record
ord-db0ca67e28ab46aa9f929a6d17638038
Source dataset
uspto-grants-1994_04
Patent number
US05302596

Reaction notes

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