Ethylamine → 5-(2,4-Bis-benzyloxy-5-tert-butyl-phenyl)-isoxazole-3-carboxylic acid ethylamide

HRID 1891167Notes

Reaction equation

HRID 1891167 reaction equation
C(O[C:4]([C:6]1[CH:10]=[C:9]([C:11]2[CH:16]=[C:15]([C:17]([CH3:20])([CH3:19])[CH3:18])[C:14]([O:21][CH2:22][C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[CH:13][C:12]=2[O:29][CH2:30][C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[O:8][N:7]=1)=[O:5])C.[CH2:37]([NH2:39])[CH3:38]>CO>[CH2:37]([NH:39][C:4]([C:6]1[CH:10]=[C:9]([C:11]2[CH:16]=[C:15]([C:17]([CH3:19])([CH3:18])[CH3:20])[C:14]([O:21][CH2:22][C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=3)=[CH:13][C:12]=2[O:29][CH2:30][C:31]2[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=2)[O:8][N:7]=1)=[O:5])[CH3:38]

Participants

4

Reactant 2

HCID 6341EthylamineHCID 247738805-(2,4-Bis-benzyloxy-5-tert-butyl-phenyl)-isoxazole-3-carboxylic acid ethyl ester

Product 1

HCID 247733555-(2,4-Bis-benzyloxy-5-tert-butyl-phenyl)-isoxazole-3-carboxylic acid ethylamide

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

5-(2,4-Bis-benzyloxy-5-tert-butyl-phenyl)-isoxazole-3-carboxylic acid ethyl ester (10.0 g, 20.6 mmol) was added to a solution of ethylamine in methanol (60 ml, 2.0M) and the suspension heated, oil bath temperature 75° C., for ˜2 hrs. The resulting solution was allowed to cool and concentrated to a pale brown oil, dichloromethane (150 ml) was added and the solution washed with water (100 ml) and saturated aqueous sodium chloride solution (75 ml). The solution was dried over anhydrous sodium sulphate and concentrated to a brown oil, solidified on standing (9.9 g, ˜quant).

Workup

  1. temperaturethe suspension heated
  2. temperatureto cool
  3. concentrationconcentrated to a pale brown oil, dichloromethane (150 ml)
  4. additionwas added
  5. washthe solution washed with water (100 ml) and saturated aqueous sodium chloride solution (75 ml)
  6. dry with materialThe solution was dried over anhydrous sodium sulphate
  7. concentrationconcentrated to a brown oil

Sources & evidence

ORD record
ord-69edd3ebfa404ce68ec9bf4e4f6d1522
Source dataset
uspto-grants-2013_08
Patent number
US08507480B2

Reaction notes

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