2-{6-[7-(1-Methyl-1-triethylsilanyloxyethyl)imidazo[1,2-alpha]pyrimidin-3-yl]pyridin-2-yl}benzonitrile → 2-{6-[7-(1-Hydroxy-1-methylethyl)imidazo[1,2-alpha]pyrimidin-3-yl]pyridin-2-yl}benzonitrile

HRID 1796037노트

반응식

HRID 1796037 반응식
[CH3:1][C:2]([C:12]1[CH:17]=[CH:16][N:15]2[C:18]([C:21]3[N:26]=[C:25]([C:27]4[CH:34]=[CH:33][CH:32]=[CH:31][C:28]=4[C:29]#[N:30])[CH:24]=[CH:23][CH:22]=3)=[CH:19][N:20]=[C:14]2[N:13]=1)([O:4][Si](CC)(CC)CC)[CH3:3]>C(O)C.Cl>[OH:4][C:2]([C:12]1[CH:17]=[CH:16][N:15]2[C:18]([C:21]3[N:26]=[C:25]([C:27]4[CH:34]=[CH:33][CH:32]=[CH:31][C:28]=4[C:29]#[N:30])[CH:24]=[CH:23][CH:22]=3)=[CH:19][N:20]=[C:14]2[N:13]=1)([CH3:1])[CH3:3]

참가 물질

4

반응물 1

HCID 695602202-{6-[7-(1-Methyl-1-triethylsilanyloxyethyl)imidazo[1,2-alpha]pyrimidin-3-yl]pyridin-2-yl}benzonitrile

생성물 1

HCID 101088622-{6-[7-(1-Hydroxy-1-methylethyl)imidazo[1,2-alpha]pyrimidin-3-yl]pyridin-2-yl}benzonitrile

시약·촉매·용매 2

HCID 313Hydrochloric Acid촉매HCID 702Ethanol용매

실험 절차

To a solution of crude 2-{6-[7-(1-methyl-1-triethylsilanyloxy-ethyl)imidazo[1,2-α]pyrimidin-3-yl]pyridin-2-yl}benzonitrile in ethanol (3 ml) was added 3 drops of concentrated hydrochloric acid and the mixture left to stir at ambient temperature for 18 h. The solvent was evaporated and the residue made basic by the addition of saturated aqueous sodium hydrogencarbonate. The aqueous phase was diluted with water (30 ml) and extracted with ethyl acetate (2×75 ml). The combined organic phase was washed with water (30 ml) and brine (30 ml), dried over anhydrous sodium sulfate, filtered and evaporated to give an orange oil. This oil was purified on silica eluting with dichloromethane (+1% 0.880 ammonia) on a gradient of methanol (1-3%). Collecting the appropriate fractions followed by recrystallisation from ethyl acetate/isohexane gave 2-{6-[7-(1-hydroxy-1-methylethyl)imidazo[1,2-α]pyrimidin-3-yl]pyridin-2-yl}benzonitrile as a white solid: δH (360 MHz, CDCl3) 1.63 (6H, s), 4.52 (1H, s), 7.16 (1H, d, J 7), 7.55-7.62 (2H, m), 7.74-7.96 (5H, m), 8.36 (1H, s), 10.37 (1H, d, J 7); m/z (ES+) 356 (M++H).

후처리

  1. waitthe mixture left
  2. customThe solvent was evaporated
  3. additionthe residue made basic by the addition of saturated aqueous sodium hydrogencarbonate
  4. additionThe aqueous phase was diluted with water (30 ml)
  5. extractionextracted with ethyl acetate (2×75 ml)
  6. washThe combined organic phase was washed with water (30 ml) and brine (30 ml)
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. customevaporated
  10. customto give an orange oil
  11. customThis oil was purified on silica eluting with dichloromethane (+1% 0.880 ammonia) on a gradient of methanol (1-3%)
  12. customCollecting the appropriate fractions
  13. customfollowed by recrystallisation from ethyl acetate/isohexane

출처 및 근거

ORD 기록
ord-0dd5c9e450054a9d86ec861e7a366ecf
출처 데이터셋
uspto-grants-2006_04
특허 번호
US07030128B2

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