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[C:1]([O:4][C:5]1[CH:14]=[C:13]2[C:8]([C:9](Cl)=[N:10][CH:11]=[N:12]2)=[CH:7][C:6]=1[O:16][CH3:17])(=[O:3])[CH3:2].[N:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[CH2:24][O:25][C:26]1[C:27]([CH3:33])=[CH:28][C:29]([NH2:32])=[CH:30][CH:31]=1>>[C:1]([O:4][C:5]1[CH:14]=[C:13]2[C:8]([C:9]([NH:32][C:29]3[CH:30]=[CH:31][C:26]([O:25][CH2:24][C:19]4[CH:20]=[CH:21][CH:22]=[CH:23][N:18]=4)=[C:27]([CH3:33])[CH:28]=3)=[N:10][CH:11]=[N:12]2)=[CH:7][C:6]=1[O:16][CH3:17])(=[O:3])[CH3:2]참가 물질
3
실험 절차
Using an analogous procedure to that described in Example 1 except that the reaction mixture was heated to reflux for 3 hours, 7-acetoxy-4-chloro-6-methoxyquinazoline was reacted with 5-amino-2-tolyl 2-pyridylmethyl ether to give 7-acetoxy-6-methoxy-4-[3-methyl-4-(2-pyridylmethoxy)anilino]quinazoline in 64% yield;
후처리
- temperaturewas heated
- temperatureto reflux for 3 hours
출처 및 근거
- ORD 기록
- ord-2670b9d7cc724f1aac0441a748810cc1
- 출처 데이터셋
- uspto-grants-1998_10
- 특허 번호
- US05821246
연결된 노트
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