4-Amino-2-chlorobenzophenone → 6-Acetoxy-4-(4-benzoyl-3-chloroanilino)quinazoline hydrochloride salt
반응식
Cl.[C:2]([O:5][C:6]1[CH:7]=[C:8]2[C:13](=[CH:14][CH:15]=1)[N:12]=[CH:11][N:10]=[C:9]2[Cl:16])(=[O:4])[CH3:3].[NH2:17][C:18]1[CH:31]=[CH:30][C:21]([C:22]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)=[O:23])=[C:20]([Cl:32])[CH:19]=1>>[ClH:16].[C:2]([O:5][C:6]1[CH:7]=[C:8]2[C:13](=[CH:14][CH:15]=1)[N:12]=[CH:11][N:10]=[C:9]2[NH:17][C:18]1[CH:31]=[CH:30][C:21]([C:22](=[O:23])[C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)=[C:20]([Cl:32])[CH:19]=1)(=[O:4])[CH3:3]참가 물질
3
실험 절차
Using an analogous procedure to that described in Example 1, 6-acetoxy-4-chloroquinazoline hydrochloride was reacted with 4-amino-2-chlorobenzophenone to give 6-acetoxy-4-(4-benzoyl-3-chloroanilino)quinazoline hydrochloride salt in 47% yield, m.p. >250° C.;
출처 및 근거
- ORD 기록
- ord-322b08e1ff5645d8b78358825d873e26
- 출처 데이터셋
- uspto-grants-1998_10
- 특허 번호
- US05821246
반응 노트
불러오는 중…