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Piperazine → 3-(1-Piperazinyl)-1,2-benzisothiazole

HRID 1489888
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인쇄 미리보기

반응식

HRID 1489888 반응식
[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[S:15]Cl)#[N:8]>ClC1C=CC=CC=1>[N:1]1([C:7]2[C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[S:15][N:8]=2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4837PiperazineHCID 110083382-cyanobenzenesulfenyl chloride

생성물 1

HCID 27721443-(1-Piperazinyl)-1,2-benzisothiazole

시약·촉매·용매 1

HCID 7964Chlorobenzene용매

반응 조건

온도
130 °C

실험 절차

86.2 g (1.00 mol) of piperazine and 7.5 g of chlorobenzene were placed in a 500 ml four-neck flask equipped with a stirrer, a thermometer, a dropping funnel and a condenser and 42.4 g (0.25 mol) of molten 2-cyanobenzenesulfenyl chloride was added dropwise thereto at about 130° C. over one hour while stirring, followed by stirring for four hours to complete the reaction. The excess piperazine was removed with water, followed by acidification with hydrochloric acid and extraction into the aqueous layer. The aqueous layer was basified with an aqueous sodium hydroxide solution to obtain 40.9 g (m.p.: 89°-90° C.) of 3-(1-piperazinyl)-1,2-benzisothiazole as crystals. The yield starting from 2-cyanobenzenesulfenyl chloride was 74.7%.

후처리

  1. customequipped with a stirrer
  2. stirringby stirring for four hours
  3. customthe reaction
  4. customThe excess piperazine was removed with water
  5. extractionfollowed by acidification with hydrochloric acid and extraction into the aqueous layer

출처 및 근거

ORD 기록
ord-24e869b1e2aa490a9682f6f2e50fe100
출처 데이터셋
uspto-grants-1997_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05679827

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