Methyl iodide → Methyl 6-(3-chloro-4-fluorobenzyl)-4-methoxy-2-methyl-3,5-dioxo-2,3,5,6,7,8-hexahydro-2,6-naphthyridine-1-carboxylate

HRID 1817333ノート

反応式

HRID 1817333 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:24]=[CH:25][C:26]=1[F:27])[CH2:5][N:6]1[CH2:15][CH2:14][C:13]2[C:8](=[C:9]([OH:22])[C:10](=[O:21])[N:11]([CH3:20])[C:12]=2[C:16]([O:18][CH3:19])=[O:17])[C:7]1=[O:23].[C:28](=O)([O-])[O-].[Cs+].[Cs+].IC>CN(C=O)C>[Cl:1][C:2]1[CH:3]=[C:4]([CH:24]=[CH:25][C:26]=1[F:27])[CH2:5][N:6]1[CH2:15][CH2:14][C:13]2[C:8](=[C:9]([O:22][CH3:28])[C:10](=[O:21])[N:11]([CH3:20])[C:12]=2[C:16]([O:18][CH3:19])=[O:17])[C:7]1=[O:23]

参加物

5

実験手順

To a solution of methyl 6-(3-chloro-4-fluorobenzyl)-4-hydroxy-2-methyl-3,5-dioxo-2,3,5,6,7,8-hexahydro-2,6-naphthyridine-1-carboxylate (7.25 g, 18 mmol) in anhydrous DMF (75 mL) was added cesium carbonate (5.98 g, 18 mmol) and iodomethane (2.86 mL, 46 mmol). The reaction was stirred at room temperature overnight, and LCMS showed 70% completion. The reaction was heated to 50° C. for 7 hours and then allowed to stir at room temperature again overnight. LCMS indicated completion. The reaction was concentrated to dryness, and the resulting residue was dissolved in chloroform. The solution was extracted twice with saturated Na2SO3 solution, dried over sodium sulfate, filtered, and evaporated to afford a dark brown oil.

後処理

  1. temperatureThe reaction was heated to 50° C. for 7 hours
  2. stirringto stir at room temperature again overnight
  3. concentrationThe reaction was concentrated to dryness
  4. dissolutionthe resulting residue was dissolved in chloroform
  5. extractionThe solution was extracted twice with saturated Na2SO3 solution
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated
  9. customto afford a dark brown oil

出典と根拠

ORDレコード
ord-5d532b35e6894c3db365dfc736f86064
出典データセット
uspto-grants-2009_10
特許番号
US07598264B2

反応ノート

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