반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:14][CH3:15])=[C:9]([O:12][CH3:13])[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:16]#[N:17].[ClH:18].N1C=CC=CC=1.[NH2:25][C:26]1[C:31](Cl)=[CH:30][CH:29]=[CH:28][C:27]=1[OH:33]>C(OCCO)C>[Cl:18][C:30]1[CH:29]=[CH:28][C:27]([OH:33])=[C:26]([NH:25][C:2]2[C:11]3[C:6](=[CH:7][C:8]([O:14][CH3:15])=[C:9]([O:12][CH3:13])[CH:10]=3)[N:5]=[CH:4][C:3]=2[C:16]#[N:17])[CH:31]=1참가 물질
5
실험 절차
Using an analogous procedure to that described in Example 286, 248.7 mg (1 mmol) of 4-chloro-6,7-dimethoxy-3-quinolinecarbonitrile in 15 mL of 2-ethoxyethanol and in the presence of 115.6 mg (1 mmol) of pyridine hydrochloride was reacted with 172.3 mg (1.2 mmol) of 2-amino-chlorophenol to give 326.4 mg (91.9%) of the product as a yellow solid, m.p.>250° C., mass (electrospray, m/e): M+H 355.8.
출처 및 근거
- ORD 기록
- ord-6fc98159b2134017892e89fd4437c5a3
- 출처 데이터셋
- uspto-grants-1999_12
- 특허 번호
- US06002008
연결된 노트
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