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Acetic Acid → Ethyl 7-chloro-1-oxo-1,2-dihydroisoquinoline-3-carboxylate

HRID 1476817
ノート
印刷プレビュー

反応式

HRID 1476817 の反応式
[H-].[Na+].[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([CH:14]=O)=[C:8]([CH:13]=1)[C:9]([O:11]C)=O.[N+:16]([CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20])#[C-].C(O)(=O)C>CN(C=O)C>[Cl:3][C:4]1[CH:13]=[C:8]2[C:7]([CH:14]=[C:18]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[NH:16][C:9]2=[O:11])=[CH:6][CH:5]=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

6

反応物 4

HCID 176Acetic AcidHCID 24758Sodium hydrideHCID 533707Ethyl isocyanoacetateHCID 58437623Methyl 5-chloro-2-formylbenzoate

生成物 1

HCID 90386855Ethyl 7-chloro-1-oxo-1,2-dihydroisoquinoline-3-carboxylate収率 31.8%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒
2 回

反応条件

温度
20 °C

実験手順

To a stirred mixture of NaH (1.81 g, 30.3 mmol) in DMF (20 mL) was added a solution of methyl 5-chloro-2-formylbenzoate (5.0 g, 25 mmol) and ethyl 2-isocyanoacetate (2.85 g, 25 mmol) in DMF (60 mL) at 40° C. over a 20 minute period. The reaction mixture was stirred at 20° C. for 2 hours. Its pH was adjusted to 7.0 with acetic acid (10%) and the mixture was extracted with DCM (3×200 mL). The organic layers were combined, washed with brine (200 mL), dried over Na2SO4, and concentrated. The crude product was purified by silica gel column chromatography eluting with petroleum ether and ethyl acetate (PE/EtOAc=15:1-5:1 gradient) to give the title compound (2.0 g, 31%). ESI-MS m/z [M+H]+252.1.

後処理

  1. extractionthe mixture was extracted with DCM (3×200 mL)
  2. washwashed with brine (200 mL)
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated
  5. customThe crude product was purified by silica gel column chromatography
  6. washeluting with petroleum ether and ethyl acetate (PE/EtOAc=15:1-5:1 gradient)

出典と根拠

ORDレコード
ord-02530edde588415687a8ebb6df7b5fc2
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09402841B2

反応ノート

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