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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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6-fluoro-7-methoxyisoquinolin-1(2H)-one → 6-fluoro-7-methoxy-3,4-dihydroisoquinolin-1(2H)-one

HRID 577447
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HRID 577447 반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[O:12][CH3:13])[C:8](=[O:14])[NH:7][CH:6]=[CH:5]2>CCO.[Pd]>[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[O:12][CH3:13])[C:8](=[O:14])[NH:7][CH2:6][CH2:5]2
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참가 물질

4

반응물 1

HCID 867236846-fluoro-7-methoxyisoquinolin-1(2H)-one

생성물 1

HCID 867236856-fluoro-7-methoxy-3,4-dihydroisoquinolin-1(2H)-one수율 80.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A suspension of 6-fluoro-7-methoxyisoquinolin-1(2H)-one (Cpd L, 0.531 g, 2.75 mmol) and 10% Pd/C in EtOH (20 mL) was stirred vigorously under a blanket of H2 (balloon) at room temperature for 2 days. The reaction mixture was filtered and the filtrate was concentrated under vacuum to give 6-fluoro-7-methoxy-3,4-dihydroisoquinolin-1(2H)-one (Cpd M, 430 mg, 80%) as a white powder.

후처리

  1. filtrationThe reaction mixture was filtered
  2. concentrationthe filtrate was concentrated under vacuum

출처 및 근거

ORD 기록
ord-38861fb43cf9460d896b1af021220119
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09040515B2

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