Sodium hydride → HCID 67429427, 화합물

HRID 1662784노트

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HRID 1662784 반응식
C([O:8][C:9](=[O:18])[NH:10][C@@H:11]([CH3:17])[C:12]([N:14]([CH3:16])[CH3:15])=[O:13])C1C=CC=CC=1.[H-].[Na+].Br[CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][N:24]=1.C([O-])(O)=O.[Na+]>CN(C=O)C>[CH3:16][N:14]([CH3:15])[C:12](=[O:13])[C@@H:11]([N:10]([CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][N:24]=1)[C:9](=[O:18])[OH:8])[CH3:17]

참가 물질

6

실험 절차

Under nitrogen atmosphere, to a solution of 2.00 g of benzyl[(1S)-2-(dimethylamino)-1-methyl-2-oxo ethyl]carbamate in DMF was added 0.33 g of NaH under ice cooling and the reaction mixture was stirred at room temperature for 10 minutes. Therein, a solution of 3.25 g of 2-(bromo methyl)pyridine in DMF (15 ml) was added, and the solution was stirred at room temperature for 3 hours. A saturated aqueous solution of NaHCO3 was added to the reaction solution, and the resulting mixture was extracted with EtOAc. The combined organic layer was washed with water and with saturated brine and dried over MgSO4, then, the drying agent was separated by filtration and the solvent was evaporated under reduced pressure. The obtained residue was purified by column chromatography (silicagel 60N, moving bed: CHCl3/EtOAc=1/1; v/v) to obtain 1.04 g of the title compound (colorless oil).

후처리

  1. stirringthe solution was stirred at room temperature for 3 hours
  2. extractionthe resulting mixture was extracted with EtOAc
  3. washThe combined organic layer was washed with water and with saturated brine
  4. dry with materialdried over MgSO4
  5. customthe drying agent was separated by filtration
  6. customthe solvent was evaporated under reduced pressure
  7. customThe obtained residue was purified by column chromatography (silicagel 60N, moving bed: CHCl3/EtOAc=1/1; v/v)

출처 및 근거

ORD 기록
ord-d0548ca44988477a90b5c3ed622cbe1a
출처 데이터셋
uspto-grants-2011_10
특허 번호
US08030499B2

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