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

HRID 245853
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HRID 245853 반응식
[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
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참가 물질

6

반응물 3

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

생성물 1

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

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-7ec3c0ae825d4f8b96b650a10b4c9233
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658646B2

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