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

HRID 1476817
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HRID 1476817 반응식
[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

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

생성물 1

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

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매
2회

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온도
20 °C

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-02530edde588415687a8ebb6df7b5fc2
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09402841B2

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