Ethylene Glycol → 4-(3-Bromo-imidazo[1,2-a]pyridin-6-ylamino)-cyclohexanol

HRID 383283노트

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HRID 383283 반응식
[O-]P([O-])([O-])=O.[K+].[K+].[K+].[Br:9][C:10]1[N:14]2[CH:15]=[C:16](I)[CH:17]=[CH:18][C:13]2=[N:12][CH:11]=1.C(O)CO.[NH2:24][C@H:25]1[CH2:30][CH2:29][C@H:28]([OH:31])[CH2:27][CH2:26]1>C(O)(C)C.[Cu]I>[Br:9][C:10]1[N:14]2[CH:15]=[C:16]([NH:24][CH:25]3[CH2:30][CH2:29][CH:28]([OH:31])[CH2:27][CH2:26]3)[CH:17]=[CH:18][C:13]2=[N:12][CH:11]=1

참가 물질

7

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온도
80 °C

실험 절차

Copper (I) iodide (0.1 eq, 1.45 g, 7.68 mmol) and potassium phosphate tribasic (2 eq, 0.153 mol, 32.5 g) are stirred at RT under an atmosphere of argon during the addition of 3-bromo-6-iodo-imidazo[1,2-a]pyridine (Intermediate F) (25 g, 77 mmol, 1 eq) in isopropyl alcohol (200 ml), ethylene glycol (2 eq, 0.153 mol, 8.5 ml) and finally trans-4-aminocyclohexanol (2 eq, 17.5 g, 153 mmol) The reaction is heated at 80° C. for 40 hours. The majority of the solvent is removed in vacuo and the residue is diluted with water (500 ml) and extracted with EtOAc (3×500 ml). The combined organic portions are dried (MgSO4) and concentrated in vacuo. Purification by flash chromatography on silica eluting with 0-15% MeOH in EtOAc gives 4-(3-bromo-imidazo[1,2-a]pyridin-6-ylamino)-cyclohexanol; [M+H]+=310 (312)

후처리

  1. customThe majority of the solvent is removed in vacuo
  2. additionthe residue is diluted with water (500 ml)
  3. extractionextracted with EtOAc (3×500 ml)
  4. dry with materialThe combined organic portions are dried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customPurification by flash chromatography on silica eluting with 0-15% MeOH in EtOAc

출처 및 근거

ORD 기록
ord-1d3cc9f3195149cf8d2fb6bce46ba202
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08367662B2

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