Dicyclohexylcarbodiimide → N-[4-(4-ethylthiophenoxy)benzyl]-2,4-dimethyl-1,3-oxazole-5-carboxamide

HRID 257853

反応式

HRID 257853 の反応式
[CH3:1][C:2]1[O:3][C:4]([C:8]([OH:10])=O)=[C:5]([CH3:7])[N:6]=1.C1(N=C=NC2CCCCC2)CCCCC1.[CH2:26]([C:28]1[CH:42]=[CH:41][C:31]([S:32][C:33]2[CH:40]=[CH:39][C:36]([CH2:37][NH2:38])=[CH:35][CH:34]=2)=[CH:30][CH:29]=1)[CH3:27]>ClCCl>[CH2:26]([C:28]1[CH:42]=[CH:41][C:31]([S:32][C:33]2[CH:40]=[CH:39][C:36]([CH2:37][NH:38][C:8]([C:4]3[O:3][C:2]([CH3:1])=[N:6][C:5]=3[CH3:7])=[O:10])=[CH:35][CH:34]=2)=[CH:30][CH:29]=1)[CH3:27]

参加物

5

実験手順

To a stirred mixture of 2,4-dimethyl-1,3-oxazole-5-carboxylic acid (155 mg, 1.1 mM) and dichloromethane (20 ml) was added 1,3-dicyclohexylcarbodiimide (227 mg, 1.1 mM) at 0°-10° C., and the mixture was stirred for 30 min at the same temperature. To this was added dropwise a solution (10 ml) of 4-(4-ethylthiophenoxy)benzylamine (285 mg, 1.1 mM) in dichloromethane, and the mixture was stirred for 12 h at room temperature. The mixture was poured into ice water, and the mixture was extracted with dichloromethane. The extract was washed with saturated ammonium chloride solution and brine, dried with magnesium sulfate, and concentrated in vacuo. The residue was chromatographed over silica gel to give N-[4-(4-ethylthiophenoxy)benzyl]-2,4-dimethyl-1,3-oxazole-5-carboxamide (164 mg, 39%) as colorless crystals, m.p. 60.0°-64.5° C.

後処理

  1. stirringthe mixture was stirred for 12 h at room temperature
  2. extractionthe mixture was extracted with dichloromethane
  3. washThe extract was washed with saturated ammonium chloride solution and brine
  4. dry with materialdried with magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe residue was chromatographed over silica gel

出典と根拠

ORDレコード
ord-9bf5f7adc5fd40939760c7953f06fb16
出典データセット
uspto-grants-1993_11
特許番号
US05264448

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