Hydrochloric Acid → 1-(3-Acetylaminopropyl)-4-benzhydrylpiperazine

HRID 280854

반응식

HRID 280854 반응식
[NH2:1][CH2:2][CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][N:8]([CH:11]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:7][CH2:6]1.[C:24](OC(=O)C)(=[O:26])[CH3:25].Cl>>[C:24]([NH:1][CH2:2][CH2:3][CH2:4][N:5]1[CH2:6][CH2:7][N:8]([CH:11]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:9][CH2:10]1)(=[O:26])[CH3:25]

참가 물질

4

반응 조건

온도
100 °C

실험 절차

A mixture of 1-(3-aminopropyl)-4-benzhydrylpiperazine (1.55 g) and acetic anhydride (16 ml) was stirred at 100° C. for 1.5 hours. The reaction mixture was concentrated and the residue was extracted with ethyl acetate. The extract was washed successively with aqueous sodium bicarbonate and water, dried and evaporated in vacuo. The residue was purified by column chromatography on silica gel eluting with ethyl acetate. The fractions containing the desired compound were combined and evaporated in vacuo to give a residue. According to a conventional manner, the residue was converted to hydrochloric acid salt, which was recrystallized from a mixture of methanol and diethyl ether to afford 1-(3-acetylaminopropyl)-4-benzhydrylpiperazine (0.8 g) as white crystals. mp: 240°-255° C. (dec.)

후처리

  1. concentrationThe reaction mixture was concentrated
  2. extractionthe residue was extracted with ethyl acetate
  3. washThe extract was washed successively with aqueous sodium bicarbonate and water
  4. customdried
  5. customevaporated in vacuo
  6. customThe residue was purified by column chromatography on silica gel eluting with ethyl acetate
  7. additionThe fractions containing the desired compound
  8. customevaporated in vacuo
  9. customto give a residue
  10. customwas recrystallized from a mixture of methanol and diethyl ether

출처 및 근거

ORD 기록
ord-a6f207cf2e004f3b945b0f31957d5aeb
출처 데이터셋
uspto-grants-1986_05
특허 번호
US04591590

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