반응식
[N:1]1[CH:6]=[CH:5][N:4]=[CH:3][C:2]=1[C:7]([NH:9][CH2:10][CH2:11][CH2:12][S:13][C:14]1[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=1)=[O:8].[ClH:20].CO>CO>[ClH:20].[ClH:20].[N:1]1[CH:6]=[CH:5][N:4]=[CH:3][C:2]=1[C:7]([NH:9][CH2:10][CH2:11][CH2:12][S:13][C:14]1[CH:15]=[CH:16][N:17]=[CH:18][CH:19]=1)=[O:8]참가 물질
4
실험 절차
To a solution of 704.5 mg (2.57 mmol) of 4-[3-(2-pyrazinecarbonylamino)propylthio]pyridine in 30 ml of methanol, 70 ml of 10% hydrochloric acid-methanol was added, and the mixture was stirred at room temperature for 2 hours. The solvent was distilled off and the residue was purified by recrystallization (solvent: ethanol-ether) to give 842.4 mg of the desired compound (85.6% yield, pale yellow crystals).
후처리
- distillationThe solvent was distilled off
- customthe residue was purified by recrystallization (solvent: ethanol-ether)
출처 및 근거
- ORD 기록
- ord-7c0a9d74a2794bf09aa140d9698f4f5f
- 출처 데이터셋
- uspto-grants-1993_09
- 특허 번호
- US05246948
연결된 노트
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