Trifluoroacetic acid → HCID 178489120, compound
Reaction equation
[CH3:1][O:2][C:3]1[N:8]=[CH:7][C:6]([C:9]2[NH:10][C:11]([CH:14]3[CH2:19][CH2:18][N:17]([CH2:20][C:21]4[CH:26]=[CH:25][C:24]([C:27]5[C:36]([C:37]6[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=6)=[CH:35][C:34]6[C:33](=[O:43])[NH:32][CH:31]=[CH:30][C:29]=6[N:28]=5)=[CH:23][CH:22]=4)[CH2:16][CH2:15]3)=[N:12][N:13]=2)=[CH:5][CH:4]=1.[C:44]([OH:50])([C:46]([F:49])([F:48])[F:47])=[O:45]>CO>[F:47][C:46]([F:49])([F:48])[C:44]([OH:50])=[O:45].[CH3:1][O:2][C:3]1[N:8]=[CH:7][C:6]([C:9]2[NH:10][C:11]([CH:14]3[CH2:19][CH2:18][N:17]([CH2:20][C:21]4[CH:22]=[CH:23][C:24]([C:27]5[C:36]([C:37]6[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=6)=[CH:35][C:34]6[C:33](=[O:43])[NH:32][CH:31]=[CH:30][C:29]=6[N:28]=5)=[CH:25][CH:26]=4)[CH2:16][CH2:15]3)=[N:12][N:13]=2)=[CH:5][CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-[4-({4-[5-(6-methoxypyridin-3-yl)-4H-1,2,4-triazol-3-yl]piperidin-1-yl}methyl)phenyl]-3-phenyl-1,6-naphthyridin-5(6H)-one (300 mg, 0.53 mmol) was dissolved in MeOH and TFA (40 μL, 0.53 mmol) was added. The solvent was evaporated under reduced pressure and the yellow residue was dried under high vacuum for 16 h to give 2-[4-({4-[5-(6-methoxypyridin-3-yl)-4H-1,2,4-triazol-3-yl]piperidin-1-yl}methyl)phenyl]-3-phenyl-1,6-naphthyridin-5(6H)-one trifluoroacetate.
Workup
- customThe solvent was evaporated under reduced pressure
- customthe yellow residue was dried under high vacuum for 16 h
Sources & evidence
- ORD record
- ord-60ec76d8a8b1467d985d336bb673b1e1
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07910561B2
Reaction notes
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