Ethyl bromoacetate → 5-(diphenylmethyl)-1-ethoxycarbonylmethyl-2(1H)-pyridinone

HRID 2389310노트

반응식

HRID 2389310 반응식
[H-].[Li+].[C:3]1([CH:9]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:10]2[CH:11]=[CH:12][C:13](=[O:16])[NH:14][CH:15]=2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.Br[CH2:24][C:25]([O:27][CH2:28][CH3:29])=[O:26]>CN(C=O)C>[C:3]1([CH:9]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:10]2[CH:11]=[CH:12][C:13](=[O:16])[N:14]([CH2:24][C:25]([O:27][CH2:28][CH3:29])=[O:26])[CH:15]=2)[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1

참가 물질

5

실험 절차

To a suspension of LiH (45.6 mg) in DMF (6.0 mL) was added portionwise 5-(diphenylmethyl)-2(1H)-pyridinone (500 mg) at ambient temperature and the mixture was stirred at the same temperature for 15 minutes. Ethyl bromoacetate (255 μL) was added dropwise to the mixture. The mixture was stirred at ambient temperature for 14 hours. The reaction was quenched with 1M HCl aqueous solution (10.0 mL) and the mixture was extracted with EtOAc (30 mL). The organic layer was washed successively with saturated NaHCO3 aqueous solution and brine, dried over anhydrous MgSO4, filtered and evaporated in vacuo. The residue was purified by silica gel column chromatography (n-hexane:EtOAc=3:2) to afford 5-(diphenylmethyl)-1-ethoxycarbonylmethyl-2(1H)-pyridinone (574 mg) as a colorless amorphous.

후처리

  1. stirringThe mixture was stirred at ambient temperature for 14 hours
  2. customThe reaction was quenched with 1M HCl aqueous solution (10.0 mL)
  3. extractionthe mixture was extracted with EtOAc (30 mL)
  4. washThe organic layer was washed successively with saturated NaHCO3 aqueous solution and brine
  5. dry with materialdried over anhydrous MgSO4
  6. filtrationfiltered
  7. customevaporated in vacuo
  8. customThe residue was purified by silica gel column chromatography (n-hexane:EtOAc=3:2)

출처 및 근거

ORD 기록
ord-8ed47085b7bf48baa4ff12f4f1b9173d
출처 데이터셋
uspto-grants-2012_09
특허 번호
US08273745B2

반응 노트

불러오는 중…