2-(N-(3,6-dichloropyridazin-4-yl)-N-methylamino)ethanol → HCID 22030726, 화합물

HRID 1421040노트

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HRID 1421040 반응식
Cl[C:2]1[N:3]=[N:4][C:5](Cl)=[CH:6][C:7]=1[N:8]([CH2:10][CH2:11][OH:12])[CH3:9]>[Pd].C(O)C.CO.N>[CH3:9][N:8]([CH2:10][CH2:11][OH:12])[C:7]1[CH:6]=[CH:5][N:4]=[N:3][CH:2]=1

참가 물질

6

실험 절차

A mixture of 2-(N-(3,6-dichloropyridazin-4-yl)-N-methylamino)ethanol (444 mg, 2 mmol) and 10% palladium-on-charcoal catalyst (150 mg) in ethanol (15 ml), methanol (5 ml) and aqueous ammonia (15 ml) was stirred under hydrogen at 3 atmospheres pressure for 4 hours. The catalyst was removed by filtration and the solvent removed from the filtrate by evaporation. The residue was dissolved in methylene chloride, the insoluble material was removed by filtration and the solvent was removed from the filtrate by evaporation. The residue was purified by column chromatography on neutral aluminum oxide eluting with methylene chloride/methanol (95/5 followed by 90/10). The purified product was triturated with petroleum ether, the solid product was collected by filtration and dried under vacuum to give 2-(N-methyl-N-(pyridazin-4-yl)amino)ethanol (275 mg, 91%).

후처리

  1. customThe catalyst was removed by filtration
  2. customthe solvent removed from the filtrate by evaporation
  3. dissolutionThe residue was dissolved in methylene chloride
  4. customthe insoluble material was removed by filtration
  5. customthe solvent was removed from the filtrate by evaporation
  6. customThe residue was purified by column chromatography on neutral aluminum oxide eluting with methylene chloride/methanol (95/5 followed by 90/10)
  7. customThe purified product was triturated with petroleum ether
  8. filtrationthe solid product was collected by filtration
  9. customdried under vacuum

출처 및 근거

ORD 기록
ord-99b061053a644923bdc954b9f0a1cb7f
출처 데이터셋
uspto-grants-2000_06
특허 번호
US06071921

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