1-(Bromomethyl)-3-(trifluoromethyl)benzene → 3-(4-Methoxy-3-methyl-benzoyl)-1-(3-trifluoromethyl-benzyl)-1H-[1,8]naphthyridin-4-one
Reaction equation
[CH3:1][O:2][C:3]1[CH:21]=[CH:20][C:6]([C:7]([C:9]2[C:18](=[O:19])[C:17]3[C:12](=[N:13][CH:14]=[CH:15][CH:16]=3)[NH:11][CH:10]=2)=[O:8])=[CH:5][C:4]=1[CH3:22].Br[CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[C:27]([C:31]([F:34])([F:33])[F:32])[CH:26]=1>>[CH3:1][O:2][C:3]1[CH:21]=[CH:20][C:6]([C:7]([C:9]2[C:18](=[O:19])[C:17]3[C:12](=[N:13][CH:14]=[CH:15][CH:16]=3)[N:11]([CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[C:27]([C:31]([F:32])([F:33])[F:34])[CH:26]=3)[CH:10]=2)=[O:8])=[CH:5][C:4]=1[CH3:22]Participants
3
Procedure
Experimental conditions analogous to those described for Step 3 of Example 1, from 50 mg (0.17 mmol) of 3-(4-Methoxy-3-methyl-benzoyl)-1H-[1,8]naphthyridin-4-one, and 1-Bromomethyl-3-trifluoromethyl-benzene 53 mg (0.22 mmol), to give 12 mg of desired compound. LCMS (M+H)+: 453.1.
Sources & evidence
- ORD record
- ord-b1b9aa6408d641a699315b3228e5c67b
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07557213B2
Reaction notes
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