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Dimethylacetamide → 7-Chloro-6-hydroxy-1-methoxyisoquinoline

HRID 1948168
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HRID 1948168 반응식
[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][N:8]=[C:9]2[O:12][CH3:13])=[CH:4][C:3]=1F.CC(N(C)C)=[O:17]>O>[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][N:8]=[C:9]2[O:12][CH3:13])=[CH:4][C:3]=1[OH:17]
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참가 물질

4

반응물 2

HCID 31374DimethylacetamideHCID 583808287-Chloro-6-fluoro-1-methoxyisoquinoline

생성물 1

HCID 1361750037-Chloro-6-hydroxy-1-methoxyisoquinoline

시약·촉매·용매 1

HCID 962Water용매

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온도
60 °C

실험 절차

A solution of sodium trimethylsilanoate (149.2 mL, 1M in THF) was added to a solution of 7-chloro-6-fluoro-1-methoxyisoquinoline (4, 10 g, 47.2 mmol) in DMA (200 mL) under argon. After stirring at 60° C. for 24 hours, the solution was evaporated under reduced pressure and then freeze dried to give crude product (20.4 g). This was dissolved in water and the pH adjusted to pH=6.5. A light brown precipitate was collected by filtration and purified by reverse phase chromatography (0 to 4 minutes, 15% acetonitrile/water, 4 to 24 minutes 15 to 90% acetonitrile/water and then 100% acetonitrile) to give 7 g of the desired product Rt=2.60 min (Method C). Detected mass: 210.0 (M+H+).

후처리

  1. customthe solution was evaporated under reduced pressure
  2. customfreeze dried
  3. customto give crude product (20.4 g)
  4. filtrationA light brown precipitate was collected by filtration
  5. custompurified by reverse phase chromatography (0 to 4 minutes, 15% acetonitrile/water, 4 to 24 minutes 15 to 90% acetonitrile/water

출처 및 근거

ORD 기록
ord-746d4314d31d4bc788a3deca4345dc46
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399482B2

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