Potassium Carbonate → HCID 67604482, compound

HRID 1419065Notes

Reaction equation

HRID 1419065 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]([CH2:18][C:19]([CH3:22])([CH3:21])[CH3:20])[C:9]([CH:11]=[CH:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])=[O:10])=[C:4]([CH:23]([OH:40])[C:24]2[CH:29]=[CH:28][C:27]([O:30][CH2:31][C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)=[CH:26][C:25]=2[O:38][CH3:39])[CH:3]=1.C(=O)([O-])[O-].[K+].[K+]>C(O)C>[CH2:31]([O:30][C:27]1[CH:28]=[CH:29][C:24]([C@@H:23]2[C:4]3[CH:3]=[C:2]([Cl:1])[CH:7]=[CH:6][C:5]=3[N:8]([CH2:18][C:19]([CH3:21])([CH3:22])[CH3:20])[C:9](=[O:10])[C@@H:11]([CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])[O:40]2)=[C:25]([O:38][CH3:39])[CH:26]=1)[C:32]1[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=1

Participants

4

Procedure

To a mixture of ethyl 3-[N-[4-chloro-2-(4-benzyloxy-α-hydroxy-2-methoxybenzyl)-phenyl]-N-neopentylcarbamoyl]acrylate (12 g), potassium carbonate (5.9 g) and ethanol (150 ml) was stirred for 24 h. After the mixture was concentrated in vacuo, the residue was diluted with water (200 ml) and extracted with ethyl acetate (200 ml). The extract was washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1) to give ethyl trans-5-(4-benzyloxy-2-methoxyphenyl)-7-chloro-1-neopentyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-acetate (9.8 g) as needles (mp=130°-131° C.).

Workup

  1. concentrationAfter the mixture was concentrated in vacuo
  2. additionthe residue was diluted with water (200 ml)
  3. extractionextracted with ethyl acetate (200 ml)
  4. washThe extract was washed with water
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1)

Sources & evidence

ORD record
ord-39f258afb60649b586bb0c16776ca3f5
Source dataset
uspto-grants-1999_03
Patent number
US05885979

Reaction notes

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