Reaction equation
[CH2:1]([O:8][C:9]1[N:10]=[N:11][CH:12]=[C:13]2[C:17]([CH3:18])=[C:16]([CH3:19])[NH:15][C:14]=12)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:20][CH:21]=[C:22]([Cl:25])[CH2:23]Cl>>[CH2:1]([O:8][C:9]1[N:10]=[N:11][CH:12]=[C:13]2[C:17]([CH3:18])=[C:16]([CH3:19])[N:15]([CH2:23][C:22]([Cl:25])=[CH:21][Cl:20])[C:14]=12)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
The title compound was prepared as ocherous powdery crystals in 8.0% yield in a similar procedure to that described in Example 41 by using 7-benzyloxy-2,3-dimethylpyrrolo[2,3-d]pyridazine and 1,2,3-trichloro-1-propene.
Sources & evidence
- ORD record
- ord-d7f0dfd88fcf48a4abe0ca993894e6d2
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06063782
Linked notes
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