Bromomethyl 4-methoxyphenyl ketone → 1-[2-(4-Methoxyphenyl)-2-oxoethyl]-4-(4-naphthalen-1-yl-butyl)piperazine

HRID 497318노트

반응식

HRID 497318 반응식
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:6]([C:7](=[O:10])[CH2:8]Br)=[CH:5][CH:4]=1.C(N(C(C)C)C(C)C)C.Cl.Cl.[C:24]1([CH2:34][CH2:35][CH2:36][CH2:37][N:38]2[CH2:43][CH2:42][NH:41][CH2:40][CH2:39]2)[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=2)[CH:27]=[CH:26][CH:25]=1>C(Cl)(Cl)Cl>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:6]([C:7](=[O:10])[CH2:8][N:41]2[CH2:40][CH2:39][N:38]([CH2:37][CH2:36][CH2:35][CH2:34][C:24]3[C:33]4[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=4)[CH:27]=[CH:26][CH:25]=3)[CH2:43][CH2:42]2)=[CH:5][CH:4]=1

참가 물질

5

실험 절차

In 6.0 ml of chloroform was dissolved 0.69 g of 4-methoxyphenacyl bromide, and 3.0 ml of N-ethyldiisopropylamine and 1.20 g of 1-(4-naphthalen-1-yl-butyl)piperazine dihydrochloride were added, followed by reflux with heating for an hour. The reaction solution was cooled to room temperature, and concentrated under reduced pressure. To the residue was added a saturated aqueous sodium bicarbonate solution and, after extraction with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate. After removal of the drying agent by filtration, the filtrate was concentrated under reduced pressure to give a crude 1-[2-(4-methoxyphenyl)-2-oxoethyl]-4-(4-naphthalen-1-yl-butyl)piperazine.

후처리

  1. additionwere added
  2. temperatureby reflux
  3. temperaturewith heating for an hour
  4. concentrationconcentrated under reduced pressure
  5. additionTo the residue was added a saturated aqueous sodium bicarbonate solution
  6. extractionafter extraction with ethyl acetate
  7. dry with materialthe organic layer was dried over anhydrous sodium sulfate
  8. customAfter removal of the drying agent
  9. filtrationby filtration
  10. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-5c20a66ae5584af3b12c9de088dc9b57
출처 데이터셋
uspto-grants-2005_09
특허 번호
US06949552B2

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