Valeryl chloride → N-[2-(7-bromo-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]methanesulfonamide

HRID 1818245노트

반응식

HRID 1818245 반응식
[NH2:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([C:11]=1[NH:12][CH2:13][CH2:14][NH:15][S:16]([CH3:19])(=[O:18])=[O:17])=[CH:9][CH:8]=[C:7]([Br:20])[CH:6]=2.[C:21](Cl)(=O)[CH2:22][CH2:23][CH2:24][CH3:25]>N1C=CC=CC=1>[Br:20][C:7]1[CH:8]=[CH:9][C:10]2[C:11]3[N:12]([CH2:13][CH2:14][NH:15][S:16]([CH3:19])(=[O:17])=[O:18])[C:21]([CH2:22][CH2:23][CH2:24][CH3:25])=[N:1][C:2]=3[CH:3]=[N:4][C:5]=2[CH:6]=1

참가 물질

4

반응물 2

HCID 61186Valeryl chlorideHCID 21984309N-[2-(3-amino-7-bromoquinolin-4-ylamino)ethyl]methanesulfonamide

생성물 1

HCID 21984119N-[2-(7-bromo-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]methanesulfonamide

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To a stirred solution of N-[2-(3-amino-7-bromoquinolin-4-ylamino)ethyl]methanesulfonamide (46.4 g, 0.129 mol) in 1000 mL pyridine was slowly added valeryl chloride (1.1 equivalents). After 1.5 hours the mixture was yellow and turbid. The reaction mixture was then heated at reflux for 12 hours, allowed to cool to ambient temperature and concentrated under reduced pressure. The residue was mostly dissolved in 10% HCl to adjust to pH 1. The resulting suspension was adjusted to pH 12 with the addtion of 50% aqueous sodium hydroxide and stirred overnight. A precipitate formed and was isolated by filtration and air-dried to provide 45 g of N-[2-(7-bromo-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]methanesulfonamide as a pale gray/green solid.

후처리

  1. temperatureThe reaction mixture was then heated
  2. temperatureat reflux for 12 hours
  3. concentrationconcentrated under reduced pressure
  4. dissolutionThe residue was mostly dissolved in 10% HCl
  5. customA precipitate formed
  6. customwas isolated by filtration
  7. customair-dried

출처 및 근거

ORD 기록
ord-1e67f52d99c24395b2c4f5639b48571d
출처 데이터셋
uspto-grants-2009_10
특허 번호
US07598382B2

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