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Methyl iodide → 5-Methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridine

HRID 546388
ノート
印刷プレビュー

反応式

HRID 546388 の反応式
[N:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[S:3][CH:2]=1.[CH3:10]I>CN(C)C=O>[CH3:10][N:6]1[CH2:7][CH2:8][C:9]2[N:1]=[CH:2][S:3][C:4]=2[CH2:5]1
参加物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 6328Methyl iodideHCID 14666228Thiazolo[5,4-c]pyridine

生成物 1

HCID 111864405-Methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridine

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Thiazolo[5,4-c]pyridine (1.61 g) was dissolved in N,N-dimethylformamide (50 ml), and to the solution methyl iodide (1.50 ml) was added, the resultant mixture was stirred at 80° C. for 4 hours. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in methanol (100 ml), sodium borohydride (1.53 g) was added, and the resultant mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, and a saturated aqueous solution of potassium carbonate and ether were added to the residue to separate an organic layer. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography on silica gel (dichloromethane:methanol 25:1) to obtain the title compound (1.28 g) as a pale yellow oil.

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. dissolutionthe residue was dissolved in methanol (100 ml)
  3. additionsodium borohydride (1.53 g) was added
  4. concentrationThe reaction mixture was concentrated under reduced pressure
  5. additiona saturated aqueous solution of potassium carbonate and ether were added to the residue
  6. customto separate an organic layer
  7. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  8. distillationthe solvent was distilled off under reduced pressure
  9. customThe residue was purified by column chromatography on silica gel (dichloromethane:methanol 25:1)

出典と根拠

ORDレコード
ord-bdedc9fc084f42eab05fab5db8c699ea
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07935824B2

反応ノート

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