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Iodine → (6-Fluoro-1-iodo-imidazo[1,5-a]pyridin-3-yl)-methanol

HRID 245853
ノート
印刷プレビュー

反応式

HRID 245853 の反応式
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:8]([CH2:11][OH:12])=[N:9][CH:10]=2)[CH:7]=1.C(=O)(O)[O-].[Na+].[I:18]I>C(O)C.O>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:8]([CH2:11][OH:12])=[N:9][C:10]=2[I:18])[CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 807IodineHCID 516892Sodium BicarbonateHCID 86677906(6-Fluoro-imidazo[1,5-a]pyridin-3-yl)-methanol

生成物 1

HCID 71280570(6-Fluoro-1-iodo-imidazo[1,5-a]pyridin-3-yl)-methanol収率 50%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

In a round-bottomed flask, (6-fluoro-imidazo[1,5-a]pyridin-3-yl)-methanol (225 mg, 1.15 mmol) was dissolved in ethanol (2 ml) and water (1 ml). Sodium bicarbonate (341 mg, 4.06 mmol) was added followed by iodine (383 mg, 1.51 mmol). The dark brown suspension was stirred at room temperature for 3 h then quenched with 10% Na2S2O3-solution and extracted with EtOAc (2×). The organic layers were washed with water and brine then dried over sodium sulfate, filtered and concentrated. The residue was absorbed on silica gel and chromatographed with EtOAc/hexanes (gradient 0-40% EtOAc) to provide 157 mg (50%, 2 steps) of (6-fluoro-1-iodo-imidazo[1,5-a]pyridin-3-yl)-methanol as a light yellow solid.

後処理

  1. customthen quenched with 10% Na2S2O3-solution
  2. extractionextracted with EtOAc (2×)
  3. washThe organic layers were washed with water and brine
  4. dry with materialthen dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was absorbed on silica gel
  8. customchromatographed with EtOAc/hexanes (gradient 0-40% EtOAc)

出典と根拠

ORDレコード
ord-7ec3c0ae825d4f8b96b650a10b4c9233
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08658646B2

反応ノート

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