Hydrochloric Acid → 2,1,3-Benzothiadiazole, 4-(1-piperazinyl)-
반응식
[N:1]1[S:2][N:3]=[C:4]2[C:9]([N:10]3[CH2:15][CH2:14][N:13](C(OC=C)=O)[CH2:12][CH2:11]3)=[CH:8][CH:7]=[CH:6][C:5]=12.Cl>C(O)C>[N:1]1[S:2][N:3]=[C:4]2[C:9]([N:10]3[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]3)=[CH:8][CH:7]=[CH:6][C:5]=12참가 물질
4
실험 절차
To a 50 ml round-bottomed flask equipped with condenser and N2 inlet were added 530 mg (1.83 mmol) 4-(2,1,3-benzothiadiazolyl)-N-vinyloxycarbonylpiperazine and 25 ml ethanol, and the suspension saturated with HCl gas. The reaction was refluxed 2.75 hours, cooled, and evaporated. The residue was triturated with acetone to give a yellow solid N-(2,1,3-benzothiadiazolyl)-piperazine, m.p. 240°-244° C., 365 mg (62%).
후처리
- customTo a 50 ml round-bottomed flask equipped with condenser and N2 inlet
- temperatureThe reaction was refluxed 2.75 hours
- temperaturecooled
- customevaporated
- customThe residue was triturated with acetone
출처 및 근거
- ORD 기록
- ord-8a0b92943bfd423badf1f35854be9455
- 출처 데이터셋
- uspto-grants-1989_05
- 특허 번호
- US04831031
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