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Ethyl 4-chloro-7-methoxyquinoline-3-carboxylate → 7-Methoxy-3-ethoxycarbonylquinoline hydrochloride

HRID 495477
노트
인쇄 미리보기

반응식

HRID 495477 반응식
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7]([Cl:18])=[C:8]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:9]=[N:10]2)=[CH:5][CH:4]=1>CCO.[Pd]>[ClH:18].[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[C:8]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:9]=[N:10]2)=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 728976Ethyl 4-chloro-7-methoxyquinoline-3-carboxylate

생성물 1

HCID 223268747-Methoxy-3-ethoxycarbonylquinoline hydrochloride

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a stirred suspension of 7-methoxy-4-chloro-3-ethoxycarbonylquinoline (Step B, 1.53 g, 5 mmol) in EtOH (15 mL) under inert atmosphere was added Pd/C 10% (153 mg). The mixture was stirred at RT under H2 (atmospheric pressure) for 2 h. The mixture was filtered and solvent removed under vacuum to give crude 7-methoxy-3-ethoxycarbonylquinoline hydrochloride.

후처리

  1. filtrationThe mixture was filtered
  2. customsolvent removed under vacuum

출처 및 근거

ORD 기록
ord-2b6b7ba4981e4432aba3692216a4cce2
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06939874B2

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