반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:13]=[CH:14][CH:15]=1)[C:5]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:6].Cl[S:17]([N:20]=C=O)(=[O:19])=[O:18]>C1(C)C=CC=CC=1>[C:5]([C:4]1[CH:3]=[C:2]([O:1][S:17](=[O:19])(=[O:18])[NH2:20])[CH:15]=[CH:14][CH:13]=1)(=[O:6])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1참가 물질
4
실험 절차
This compound was prepared according to the procedure used in Example 84. A mixture of 9.9 g (0.05 mole) of 3-hydroxybenzophenone and 4.4 ml (7.1 g, 0.0505 mole) of chlorosulfonyl isocyanate in 75 ml of toluene gave a solid as residue. This residue was recrystallized successively from benzene and then methylene chloride to yield 4.2 g (30%) of the title compound as a white solid, mp 72°-74° C.
후처리
- customThis compound was prepared
- customgave a solid as residue
- customThis residue was recrystallized successively from benzene
출처 및 근거
- ORD 기록
- ord-b0db0bc544d84fe2901daa810e56f1bf
- 출처 데이터셋
- uspto-grants-1993_12
- 특허 번호
- US05273993
연결된 노트
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