2-Chloroimidazoline sulfate → 2-[4-(1-Benzenesulfonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline

HRID 1358846노트

반응식

HRID 1358846 반응식
[C:1]1([S:7]([N:10]2[CH2:15][CH2:14][CH:13]([CH2:16][C:17]3[CH:22]=[CH:21][C:20]([NH2:23])=[CH:19][CH:18]=3)[CH2:12][CH2:11]2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(O)(O)(=O)=O.Cl[C:30]1[NH:31][CH2:32][CH2:33][N:34]=1>CC(O)C>[C:1]1([S:7]([N:10]2[CH2:15][CH2:14][CH:13]([CH2:16][C:17]3[CH:18]=[CH:19][C:20]([NH:23][C:30]4[NH:34][CH2:33][CH2:32][N:31]=4)=[CH:21][CH:22]=3)[CH2:12][CH2:11]2)(=[O:8])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

참가 물질

4

실험 절차

A mixture of 4-(1-benzenesulfonylpiperidin-4-ylmethyl)-phenylamine (0.28 g, 0.83 mmol) and 2-chloro-2-imidazoline sulfate (0.25 g, 1.25 mmol) in 2-propanol (20 mL) was heated under reflux for 30 minutes under nitrogen atmosphere. The reaction mixture was concentrated in vacuo. The residue was basified with 10% sodium hydroxide solution and extracted with dichloromethane. The organic layer was washed with cold water and brine, dried, and solvents removed in vacuo. The residue was chromatographed on neutral aluminum oxide, eluting with 1% methanol/dichloromethane, to give 2-[4-(1-benzenesulfonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline (0.29 g, 89%) as a foam. Analysis for C21H26N4O2S•5H2O: Calc.: C, 61.89; H, 6.68; N, 13.75; Found: C,62.00; H, 6.52; N, 13.85.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 30 minutes under nitrogen atmosphere
  3. concentrationThe reaction mixture was concentrated in vacuo
  4. extractionextracted with dichloromethane
  5. washThe organic layer was washed with cold water and brine
  6. customdried
  7. customsolvents removed in vacuo
  8. customThe residue was chromatographed on neutral aluminum oxide
  9. washeluting with 1% methanol/dichloromethane

출처 및 근거

ORD 기록
ord-3554434d4f3e4212b693876daeff2d19
출처 데이터셋
uspto-grants-2003_07
특허 번호
US06596876B2

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