Diethyl Ether → HCID 20375614, 화합물

HRID 1448821노트

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HRID 1448821 반응식
[H-].[Na+].[Cl:3][C:4]1[CH:22]=[CH:21][C:7]([CH2:8][N:9]2[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[C:12]([CH3:19])=[CH:11][C:10]2=[O:20])=[CH:6][CH:5]=1.[C:23](OCC)(=[O:29])[C:24]([O:26][CH2:27][CH3:28])=[O:25].CCOCC>CN(C)C=O>[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([CH2:8][N:9]2[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[C:12]([CH2:19][C:23](=[O:29])[C:24]([O:26][CH2:27][CH3:28])=[O:25])=[CH:11][C:10]2=[O:20])=[CH:21][CH:22]=1

참가 물질

6

실험 절차

Sodium hydride (18 g.; 60% w/w dispersion in oil, washed as described in Example 1) was stirred in dry dimethylformamide (300 ml.), and 1-(4-chlorobenzyl)-1,2-dihydro-4-methyl-2-oxoquinoline (64.7 g.) was added, followed by diethyl oxalate (55 g.). The mixture was stirred at room temperature for 2.5 hours with occasional external cooling to keep the temperature below 25° C. Ether (2 l.) was added, and the mixture was filtered. The solid residue was washed with ether (500 ml.), and then suspended in dimethylformamide (200 ml.) and acidified to pH 2 by the addition of concentrated hydrochloric acid. The resultant mixture was added to water (3 l.), and the mixture filtered, and the solid residue washed with water (2 l.), drained well, and crystallised from ethanol to give ethyl 1-(4-chlorobenzyl)-1,2-dihydro-2-oxoquinol-4-ylpyruvate, m.p. 180°-182° C.

후처리

  1. temperatureexternal cooling
  2. customthe temperature below 25° C
  3. filtrationthe mixture was filtered
  4. washThe solid residue was washed with ether (500 ml.)
  5. additionacidified to pH 2 by the addition of concentrated hydrochloric acid
  6. additionThe resultant mixture was added to water (3 l.)
  7. filtrationthe mixture filtered
  8. washthe solid residue washed with water (2 l.)
  9. customcrystallised from ethanol

출처 및 근거

ORD 기록
ord-e612258b74744da1aaed3ac7a4f8b10f
출처 데이터셋
uspto-grants-1980_02
특허 번호
US04187310

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