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Dimethyl (4-methoxy-2-nitrobenzyl)malonate → 7-Methoxy-2-oxo-1,2,3,4-tetrahydro-3-quinolinecarboxylic acid

HRID 2269725
ノート
印刷プレビュー

反応式

HRID 2269725 の反応式
[CH3:1][O:2][C:3]1[CH:18]=[CH:17][C:6]([CH2:7][CH:8]([C:13]([O:15]C)=[O:14])[C:9](OC)=[O:10])=[C:5]([N+:19]([O-])=O)[CH:4]=1>[C].[Pd].C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:6]([CH2:7][CH:8]([C:13]([OH:15])=[O:14])[C:9](=[O:10])[NH:19]2)=[CH:17][CH:18]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 53955072Dimethyl (4-methoxy-2-nitrobenzyl)malonate

生成物 1

HCID 229986197-Methoxy-2-oxo-1,2,3,4-tetrahydro-3-quinolinecarboxylic acid収率 82.7%

試薬・触媒・溶媒 2

HCID 178418390HCID 178418390、化合物触媒HCID 702Ethanol溶媒

反応条件

温度
80 °C

実験手順

10% Palladium- carbon (2.0 g) was added to an ethanol (200 ml) solution of dimethyl (4-methoxy-2-nitrobenzyl)malonate (19 g), and catalytic hydrogenation was conducted at room temperature under an atmospheric pressure for 24 hours. The reaction mixture was further stirred at 80° C. for 24 hours. The catalyst was removed by filtration, and the filtrate was concentrated. The residue was dissolved in a mixed solvent of THF (250 ml) and methanol (250 ml), to which was added dropwise 1N aqueous sodium hydroxide solution (126 ml) under ice-cooling. The reaction mixture was stirred at room temperature for 72 hours and concentrated. 1N Hydrochloric acid was added to the residue to make acidic, and the precipitated crystals were collected by filtration. The obtained crude crystals were washed with acetone to give the entitled compound (11.7 g).

後処理

  1. customThe catalyst was removed by filtration
  2. concentrationthe filtrate was concentrated
  3. dissolutionThe residue was dissolved in a mixed solvent of THF (250 ml) and methanol (250 ml), to which
  4. additionwas added dropwise 1N aqueous sodium hydroxide solution (126 ml) under ice-
  5. temperaturecooling
  6. stirringThe reaction mixture was stirred at room temperature for 72 hours
  7. concentrationconcentrated
  8. addition1N Hydrochloric acid was added to the residue
  9. filtrationthe precipitated crystals were collected by filtration
  10. customThe obtained crude crystals
  11. washwere washed with acetone

出典と根拠

ORDレコード
ord-3bf3cda12c274e63835b766fbd46b69a
出典データセット
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06329389B1

反応ノート

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