Reaction equation
Cl[C:2]1[C:3]([C:10]([O:12][CH3:13])=[O:11])=[N:4][N:5]([CH3:9])[C:6](=[O:8])[CH:7]=1.[F:14][C:15]1[CH:21]=[CH:20][CH:19]=[CH:18][C:16]=1[NH2:17]>>[F:14][C:15]1[CH:21]=[CH:20][CH:19]=[CH:18][C:16]=1[NH:17][C:2]1[C:3]([C:10]([O:12][CH3:13])=[O:11])=[N:4][N:5]([CH3:9])[C:6](=[O:8])[CH:7]=1Participants
3
Procedure
The title compound was prepared in 61% yield by the procedure as previously described in Example 166 (step H) using methyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylate (109 mg, 0.54 mmol, prepared as previously described in Example 1 (steps A-G) and 2-fluoroaniline (0.053 mL, 0.54 mmol).
Workup
- customprepared
Sources & evidence
- ORD record
- ord-e3d3226b93d840e1a9ed91970ad037b0
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07732616B2
Linked notes
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