Thionyl Chloride → 6-benzyloxy-N-(5-chloropentyl)-3-nitroquinolin-4-amine

HRID 598316노트

반응식

HRID 598316 반응식
S(Cl)([Cl:3])=O.[CH2:5]([O:12][C:13]1[CH:14]=[C:15]2[C:20](=[CH:21][CH:22]=1)[N:19]=[CH:18][C:17]([N+:23]([O-:25])=[O:24])=[C:16]2[NH:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31]O)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1>ClCCl>[CH2:5]([O:12][C:13]1[CH:14]=[C:15]2[C:20](=[CH:21][CH:22]=1)[N:19]=[CH:18][C:17]([N+:23]([O-:25])=[O:24])=[C:16]2[NH:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][Cl:3])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1

참가 물질

4

실험 절차

Under a nitrogen atmosphere, thionyl chloride (1.7 mL, 23 mmol) was added to a mixture of 5-{[6-(benzyloxy)-3-nitroquinolin-4-yl]amino}pentan-1-ol (5.95 g, 15.6 mmol) and anhydrous dichloromethane (78 mL). The reaction became homogeneous and was heated at reflux for 1.5 hours, at which time a yellow precipitate formed. The volatiles were removed under reduced pressure, and the residue was partitioned between dilute aqueous sodium carbonate (100 mL) and dichloromethane (150 mL). The aqueous layer was washed with dichloromethane (50 mL), and the combined organic solutions were washed with brine (50 mL), dried over sodium sulfate, filtered, and concentrated under reduced pressure to provide 6.24 g of 6-benzyloxy-N-(5-chloropentyl)-3-nitroquinolin-4-amine as a yellow oil.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 1.5 hours, at which time a yellow precipitate
  3. customformed
  4. customThe volatiles were removed under reduced pressure
  5. customthe residue was partitioned between dilute aqueous sodium carbonate (100 mL) and dichloromethane (150 mL)
  6. washThe aqueous layer was washed with dichloromethane (50 mL)
  7. washthe combined organic solutions were washed with brine (50 mL)
  8. dry with materialdried over sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-4b1b7aacfc3244129dd69ce994cae70e
출처 데이터셋
uspto-grants-2011_03
특허 번호
US07897597B2

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