3-Fluoro-6-(methylamino)pyridine → Methyl 5-chloro-2-{[(5-fluoropyridin-2-yl)(methyl)amino]methyl}benzoate
Reaction equation
BrC[CH2:3][C:4]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][C:5]=1[C:6]([O:8][CH3:9])=[O:7].[F:15][C:16]1[CH:17]=[CH:18][C:19]([NH:22][CH3:23])=[N:20][CH:21]=1>>[Cl:14][C:11]1[CH:12]=[CH:13][C:4]([CH2:3][N:22]([C:19]2[CH:18]=[CH:17][C:16]([F:15])=[CH:21][N:20]=2)[CH3:23])=[C:5]([CH:10]=1)[C:6]([O:8][CH3:9])=[O:7]Participants
3
Procedure
The title compound was prepared according to the procedure described in step 1 of Example 22 from methyl 2-(bromoethyl)-5-chlorobenzoate and 5-fluoro-N-methylpyridin-2-amine (step 1):
Sources & evidence
- ORD record
- ord-0830156bfebd48ca989a2ccdc2d782dc
- Source dataset
- uspto-grants-2009_05
- Patent number
- US07534914B2
Reaction notes
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