Nitrogen → HCID 22025594, 화합물

HRID 396594노트

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HRID 396594 반응식
N#N.Br[C:4]1[C:5]([O:13][CH3:14])=[CH:6][C:7]([OH:12])=[C:8]([CH:11]=1)[CH:9]=[O:10].[S:15]1[CH:19]=[CH:18][CH:17]=[C:16]1B(O)O.C([O-])([O-])=O.[Na+].[Na+]>COCCOC>[S:15]1[C:19]([C:4]2[C:5]([O:13][CH3:14])=[CH:6][C:7]([OH:12])=[C:8]([CH:11]=2)[CH:9]=[O:10])=[CH:18][C:17]2[CH:5]=[CH:4][CH:11]=[CH:8][C:16]1=2

참가 물질

6

실험 절차

Ex-62B: A stream of N2 was bubbled through a solution of 5-bromo-2-hydroxy-4-methoxybenzaldehyde (1 g, 4.3 mmol) from Ex-62A in 30 mL of ethylene glycol dimethyl ether for 15 min. Tetrakis-triphenylphosphine palladium (0) (0.5 g, 0.4 mmol) was added along with thiophene-2-boronic acid (1.2 g, 6.5 mmol) and 10 mL of Na2CO3 (2M aqueous solution). The resulting mixture was stirred under reflux overnight. The solvent was removed by rotary evaporation and the residue was treated with saturated NaHCO3 and extracted with dichloromethane. The organic phase was washed with brine, dried over MgSO4, and filtered to remove drying agent. Solvent was removed by rotary evaporation. Purification of the crude material by silica gel chromatography (hexanes/EtOAc, 2:1) gave 1.04 g of the desired 5-benzo[b]thien-2-yl-2-hydroxy-4-methoxybenzaldehyde.

후처리

  1. temperatureunder reflux overnight
  2. customThe solvent was removed by rotary evaporation
  3. additionthe residue was treated with saturated NaHCO3
  4. extractionextracted with dichloromethane
  5. washThe organic phase was washed with brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customto remove
  9. customdrying agent
  10. customSolvent was removed by rotary evaporation
  11. customPurification of the crude material by silica gel chromatography (hexanes/EtOAc, 2:1)

출처 및 근거

ORD 기록
ord-6d24c9270c8444baa03a6173ce021793
출처 데이터셋
uspto-grants-2003_08
특허 번호
US06608101B1

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