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1-Phenylpiperazine → 1-(Naphthalen-2-ylmethyl)-4-phenylpiperazine

HRID 1288565
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인쇄 미리보기

반응식

HRID 1288565 반응식
Cl[CH2:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=1.C(=O)([O-])[O-].[Na+].[Na+].[CH:19]1[CH:20]=[CH:21][C:22]([N:25]2[CH2:30][CH2:29][NH:28][CH2:27][CH2:26]2)=[CH:23][CH:24]=1>CN(C)C=O>[CH:4]1[C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH:11]=[CH:12][C:3]=1[CH2:2][N:28]1[CH2:29][CH2:30][N:25]([C:22]2[CH:23]=[CH:24][CH:19]=[CH:20][CH:21]=2)[CH2:26][CH2:27]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 70961-PhenylpiperazineHCID 10340Sodium CarbonateHCID 756322-(Chloromethyl)naphthalene

생성물 1

HCID 2878041-(Naphthalen-2-ylmethyl)-4-phenylpiperazine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of 10.0 g. of β-chloromethylnapthalene, 6.0 g. of sodium carbonate and 9.0 g. of phenylpiperazine in 60 ml. of dimethylformamide is stirred under nitrogen on a steambath for five hours. The reaction mixture is then cooled and filtered. The filtrate is concentrated and stirred with ice water. The formed precipitate is filtered off, dissolved in isobutyl alcohol and treated with ethereal hydrogen chloride to yield the hydrochloride salt of 1-(β-napthylmethyl)-4-(phenyl)piperazine having a melting point of 226°-228° C.

후처리

  1. additionA mixture of 10.0 g
  2. temperatureThe reaction mixture is then cooled
  3. filtrationfiltered
  4. concentrationThe filtrate is concentrated
  5. filtrationThe formed precipitate is filtered off
  6. dissolutiondissolved in isobutyl alcohol
  7. additiontreated with ethereal hydrogen chloride

출처 및 근거

ORD 기록
ord-b50ac38330f74f7494d55c0576370cb9
출처 데이터셋
uspto-grants-1976_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03988457

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