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HCID 58216632、化合物 → 3-Hydroxy-6-methoxy-3,4-dihydro-1,5-naphthyridin-2(1H)-one

HRID 1799572
ノート
印刷プレビュー

反応式

HRID 1799572 の反応式
[OH:1][CH:2]([CH2:8][C:9]1[C:14]([N+:15]([O-])=O)=[CH:13][CH:12]=[C:11]([O:18][CH3:19])[N:10]=1)[C:3](OCC)=[O:4].[H][H]>CO.[Pd]>[OH:1][CH:2]1[CH2:8][C:9]2[C:14](=[CH:13][CH:12]=[C:11]([O:18][CH3:19])[N:10]=2)[NH:15][C:3]1=[O:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 58216632HCID 58216632、化合物HCID 178418361HCID 178418361、化合物

生成物 1

HCID 534147233-Hydroxy-6-methoxy-3,4-dihydro-1,5-naphthyridin-2(1H)-one

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

A roundbottom flask was charged with a solution of ethyl 2-hydroxy-3-(6-methoxy-3-nitropyridin-2-yl)propanoate (37 mmol) in methanol (500 ml). To the mixture was added 10% palladium on carbon (3 g). The solution was shaken under 40 psi of hydrogen for 12 hours. The resulting solution was then allowed to react, with stirring, for 5 hours while the temperature was maintained at room temperature. The mixture was then filtered and the filtrate was diluted with 100 ml of water. Hydrochloric acid was added until the pH=5. The mixture was filtered and the filtrate was adjusted to pH=8 by the addition of sodium carbonate. The solids that formed were collected by filtration to afford the title compound.

後処理

  1. customto react
  2. filtrationThe mixture was then filtered
  3. additionthe filtrate was diluted with 100 ml of water
  4. additionHydrochloric acid was added until the pH=5
  5. filtrationThe mixture was filtered
  6. additionthe filtrate was adjusted to pH=8 by the addition of sodium carbonate
  7. customThe solids that formed
  8. filtrationwere collected by filtration

出典と根拠

ORDレコード
ord-583e44e57fbc447db3003efe723ba0cf
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08344144B2

反応ノート

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