반응식
[C:1]([C:3]1([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([OH:15])[CH:10]=2)[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1)#[N:2].[CH3:16][C:17]1[N:18]([C:22]2[CH:29]=[CH:28][C:25]([CH2:26]Cl)=[CH:24][CH:23]=2)[CH:19]=[CH:20][N:21]=1>>[C:1]([C:3]1([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH2:26][C:25]3[CH:24]=[CH:23][C:22]([N:18]4[CH:19]=[CH:20][N:21]=[C:17]4[CH3:16])=[CH:29][CH:28]=3)[CH:10]=2)[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1)#[N:2]참가 물질
3
실험 절차
4-Cyano-4-(3-hydroxyphenyl)-3,4,5,6-tetrahydro-2H-pyran was reacted with 4-(2-methylimidazol-1-yl)benzylchloride to give the titled compound in 38% yield as colorless needles according to the procedure described in Example 2H.
출처 및 근거
- ORD 기록
- ord-b4274353fdeb485aa342c7369e3dbcc5
- 출처 데이터셋
- uspto-grants-1999_03
- 특허 번호
- US05883106
연결된 노트
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