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

HRID 45207
ノート
印刷プレビュー

反応式

HRID 45207 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
60 °C

実験手順

A solution of sodium trimethylsilanoate (149.2 mL, 1M in THF) was added to a solution of 7-chloro-6-fluoro-1-methoxyisoquinoline (10, 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 2). Detected mass: 210.0 (M+H+).

後処理

  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

出典と根拠

ORDレコード
ord-1084423b357245748455875f1a38a7aa
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08541449B2

反応ノート

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