Lithium hydroxide, monohydrate → 5-Fluoro-6-hydroxypyridine-3-carboxylic acid

HRID 2370824ノート

反応式

HRID 2370824 の反応式
[F:1][C:2]1[C:7](=[O:8])[NH:6][CH:5]=[C:4]([C:9]([O:11]C)=[O:10])[CH:3]=1.O.[OH-].[Li+]>CO.O>[F:1][C:2]1[C:7](=[O:8])[NH:6][CH:5]=[C:4]([C:9]([OH:11])=[O:10])[CH:3]=1

参加物

5

実験手順

To a solution of methyl 5-fluoro-6-oxo-1,6-dihydropyridine-3-carboxylate (0.876 g, 5.12 mmol) in MeOH (33 mL) and water (11 mL), was added lithium hydroxide hydrate (1.074 g, 25.6 mmol). The resulting mixture was then stirred at rt for 5 h. The mixture was concentrated and the pH was adjusted to pH=5 using concentrated HCl. The mixture was then concentrated and dried in vacuo. The resulting residue was dissolved in MeOH (20 mL) and silica gel was added. The mixture was concentrated and dried. The solid mixture was then purified by silica gel flash column chromatography (30%-100% EtOAc/hexane, then 0%-100% MeOH/DCM) to give the title compound as an off-white solid. MS (ESI, positive ion) m/z: 158 (M+H).

後処理

  1. concentrationThe mixture was concentrated
  2. concentrationThe mixture was then concentrated
  3. customdried in vacuo
  4. dissolutionThe resulting residue was dissolved in MeOH (20 mL)
  5. additionsilica gel was added
  6. concentrationThe mixture was concentrated
  7. customdried
  8. customThe solid mixture was then purified by silica gel flash column chromatography (30%-100% EtOAc/hexane

出典と根拠

ORDレコード
ord-f0e0a5ecf47e446f9476fa7de850cdfe
出典データセット
uspto-grants-2014_04
特許番号
US08710043B2

反応ノート

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