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1-Benzylpiperazine → HCID 23155694, 화합물

HRID 1714800
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HRID 1714800 반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([Cl:12])[CH:10]=2)[CH:5]=[CH:4][N:3]=1.[CH2:13]([N:20]1[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>O>[CH2:13]([N:20]1[CH2:25][CH2:24][N:23]([C:2]2[C:11]3[C:6](=[CH:7][CH:8]=[C:9]([Cl:12])[CH:10]=3)[CH:5]=[CH:4][N:3]=2)[CH2:22][CH2:21]1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 759941-BenzylpiperazineHCID 6409561,7-Dichloroisoquinoline

생성물 1

HCID 23155694HCID 23155694, 화합물수율 71%

시약·촉매·용매 1

HCID 962Water용매

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온도
150 °C

실험 절차

A mixture of 3.96 g 1,7-dichloroisoquinoline and 10.50 g of benzylpiperazine was stirred at 150° C. for 3 hours. To the residue water was added, followed by extraction with chloroform, washing with saturated aqueous sodium hydrogencarbonate solution and drying over anhydrous magnesium sulfate. Distilling the solvent off under reduced pressure, the residue was purified on silica gel column chromatography (ethyl acetate) to provide 4.78 g (71%) of 1-(4-benzylpiperazin-1-yl)-7-chloroisoquinoline.

후처리

  1. extractionfollowed by extraction with chloroform
  2. washwashing with saturated aqueous sodium hydrogencarbonate solution
  3. dry with materialdrying over anhydrous magnesium sulfate
  4. distillationDistilling the solvent off under reduced pressure
  5. customthe residue was purified on silica gel column chromatography (ethyl acetate)

출처 및 근거

ORD 기록
ord-7e3ad9cdbd824d7380289754968da568
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07799775B2

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