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Sodium hydride → Ethyl 8-chloro-1-oxo-1,2-dihydroisoquinoline-3-carboxylate

HRID 1476823
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HRID 1476823 반응식
[H-].[Na+].[Cl:3][C:4]1[CH:13]=[CH:12][CH:11]=[C:10]([CH:14]=O)[C:5]=1[C:6]([O:8]C)=O.[N+:16]([CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20])#[C-]>CN(C=O)C.CCOC(C)=O>[Cl:3][C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[C:6](=[O:8])[NH:16][C:18]([C:19]([O:21][CH2:22][CH3:23])=[O:20])=[CH:14]2
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참가 물질

6

반응물 3

HCID 24758Sodium hydrideHCID 533707Ethyl isocyanoacetateHCID 53408620Methyl 2-chloro-6-formyl-benzoate

생성물 1

HCID 90386899Ethyl 8-chloro-1-oxo-1,2-dihydroisoquinoline-3-carboxylate수율 15.6%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매2회
HCID 8857
Ethyl Acetate
용매

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온도
20 °C

실험 절차

To a solution of NaH (652.8 mg, 16.32 mmol) in DMF (20 mL) was added methyl 2-chloro-6-formylbenzoate (2.7 g, 13.6 mmol) and ethyl 2-isocyanoacetate (1.55 g, 13.6 mmol) in DMF (5 mL) at 40° C. over a 20 minute period. The reaction mixture was stirred at 20° C. for an additional 30 minutes. The reaction mixture was subsequently diluted with EtOAc (100 mL) and washed with saturated aqueous Na2CO3. The organic phase was concentrated in vacuo. The crude product was purified by column chromatography eluting with a gradient of EtOAc (0-90%) and PE to give the title compound (0.5 g, 15.6%). ESI-MS m/z [M+H]+ 252.1.

후처리

  1. washwashed with saturated aqueous Na2CO3
  2. concentrationThe organic phase was concentrated in vacuo
  3. customThe crude product was purified by column chromatography
  4. washeluting with a gradient of EtOAc (0-90%) and PE

출처 및 근거

ORD 기록
ord-0440bd35943b449096a6b089816df378
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09402841B2

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