Ethyl iodoacetate → (1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl ester

HRID 406482

反応式

HRID 406482 の反応式
[C:1]1(=[O:11])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][NH:2]1.[H-].[Na+].I[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17]>C1(C)C=CC=CC=1>[CH2:19]([O:18][C:16](=[O:17])[CH2:15][N:2]1[CH2:3][CH2:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[C:1]1=[O:11])[CH3:20]

参加物

5

反応物 3

HCID 12183Ethyl iodoacetateHCID 24758Sodium hydrideHCID 1508963,4-dihydroisoquinolin-1(2H)-one

生成物 1

HCID 59764846(1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl ester

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

To a solution of 3,4-dihydro-2H-isoquinolin-1-one (0.250 g, 1.70 mmol) in toluene (5 mL) was added sodium hydride (60% in mineral oil, 0.049 g, 2.04 mmol) and the resulting suspension was heated at about reflux for about 1 h. The reaction mixture was cooled at room temperature and ethyl 2-iodoacetate (0.364 g, 1.70 mmol) was added dropwise and the mixture was again heated at about reflux for about 12 h. The reaction mixture was cooled at room temperature and filtered, rinsed with toluene. The filtrate was concentrated in vacuo to provide (1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl ester as a peach oil (0.336 g, 1.44 mmol). The crude material was used in subsequent reactions without further purification.

後処理

  1. temperaturethe resulting suspension was heated at
  2. temperatureabout reflux for about 1 h
  3. temperaturethe mixture was again heated at
  4. temperatureabout reflux for about 12 h
  5. temperatureThe reaction mixture was cooled at room temperature
  6. filtrationfiltered
  7. washrinsed with toluene
  8. concentrationThe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-1d1de92b70de414f8fecb0ebfe936e74
出典データセット
uspto-grants-2014_06
特許番号
US08754107B2

関連ノート

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