반응식
[H-].[Na+].[OH:3][CH2:4][CH2:5][CH2:6][S:7]([NH2:10])(=[O:9])=[O:8].Cl[C:12]1[CH:13]=[CH:14][C:15]2[N:16]([N:18]=[CH:19][N:20]=2)[N:17]=1.Cl.[Cl-].[Na+]>CN(C)C=O>[S:7]([CH2:6][CH2:5][CH2:4][O:3][C:12]1[CH:13]=[CH:14][C:15]2[N:16]([N:18]=[CH:19][N:20]=2)[N:17]=1)(=[O:9])(=[O:8])[NH2:10]참가 물질
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
In 12 ml of dimethylformamide was suspended 0.48 g of 60% sodium hydride in oil followed by addition of 0.835 g of 3-hydroxy-1-propanesulfonamide and the mixture was stirred under reduced pressure at room temperature for 30 minutes. Then, 0.928 g of 6-chloro[1,2,4]triazolo[1,5-b]pyridazine was added and the mixture was further stirred at room temperature for 18 hours. Following addition of 40 ml of ice water, the reaction mixture was adjusted to pH6 with 1N-hydrochloric acid then saturated with sodium chloride. The aqueous layer was extracted with tetrahydrofuran and the extract was dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was crystallized from ethyl ether. The washed crystals were recrystallized from hot methanol to provide 0.811 g of title compound. m.p. 145°-147° C.
후처리
- stirringthe mixture was further stirred at room temperature for 18 hours
- extractionThe aqueous layer was extracted with tetrahydrofuran
- dry with materialthe extract was dried over magnesium sulfate
- distillationThe solvent was distilled off under reduced pressure
- customthe resulting residue was crystallized from ethyl ether
- customThe washed crystals were recrystallized from hot methanol
출처 및 근거
- ORD 기록
- ord-ef5441d25a9b42f7b19df8c1f2556881
- 출처 데이터셋
- uspto-grants-1995_02
- 특허 번호
- US05389633
연결된 노트
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