Bromine → 6-Benzylsulfamoyl-2-bromo-5-chloro-1-indanone
반응식
[CH2:1]([NH:8][S:9]([C:12]1[CH:20]=[C:19]2[C:15]([CH2:16][CH2:17][C:18]2=[O:21])=[CH:14][C:13]=1[Cl:22])(=[O:11])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Br:23]Br>C(O)(=O)C>[CH2:1]([NH:8][S:9]([C:12]1[CH:20]=[C:19]2[C:15]([CH2:16][CH:17]([Br:23])[C:18]2=[O:21])=[CH:14][C:13]=1[Cl:22])(=[O:11])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
4
실험 절차
According to Example 1 e), 10.05 g (30 mmoles) of 6-benzylsulfamoyl-5-chloro-1-indanone and 4.8 g (30 mmoles) of bromine in a total of 110 ml of glacial acetic acid yield the substance having a melting point of from 159° to 161° C. which after reprecipitation from a mixture of ethyl acetate and petroleum ether has a melting point in the range of from 176° to 178° C.
후처리
- customyield the substance
- customof from 159° to 161° C. which
- customafter reprecipitation
- additionfrom a mixture of ethyl acetate and petroleum ether
- customof from 176° to 178° C.
출처 및 근거
- ORD 기록
- ord-3e4523ab0b9d414fb5d47053c1926807
- 출처 데이터셋
- uspto-grants-1978_12
- 특허 번호
- US04129656
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