Trifluoroacetic acid → N-(4-{3-[4-(2,3-Difluoro-phenyl)-isoxazol-5-yl]-1H-pyrrolo[2,3-b]pyridin-5-yl}-cyclohex-3-enyl)-methanesulfonamide
Reaction equation
[F:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[CH:4][C:3]=1[C:9]1[CH:10]=[N:11][O:12][C:13]=1[C:14]1[C:22]2[C:17](=[N:18][CH:19]=[C:20]([C:23]3[CH2:28][CH2:27][CH:26]([NH2:29])[CH2:25][CH:24]=3)[CH:21]=2)[NH:16][CH:15]=1.N1([O:39][S:40]([CH3:43])(=O)=[O:41])C2C=CC=CC=2N=N1.C(O)(C(F)(F)F)=O>CN(C=O)C.CCN(C(C)C)C(C)C>[F:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[CH:4][C:3]=1[C:9]1[CH:10]=[N:11][O:12][C:13]=1[C:14]1[C:22]2[C:17](=[N:18][CH:19]=[C:20]([C:23]3[CH2:28][CH2:27][CH:26]([NH:29][S:40]([CH3:43])(=[O:41])=[O:39])[CH2:25][CH:24]=3)[CH:21]=2)[NH:16][CH:15]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 4-{3-[4-(2,3-Difluoro-phenyl)-isoxazol-5-yl]-1H-pyrrolo [2,3-b]pyridin-5-yl}-cyclohex-3-enylamine (47 mg, 0.12 mmol) in DMF (2 ml) was added methanesulfonic acid benzotriazol-1-yl ester (27 mg, 0.13 mmol) and Hunig base (10 drops) and stirred for 1 h. TFA was added, and the reaction mixture was purified by HPLC to give the methanesulfonamide (25.9 mg) in 46% yield.
Workup
- customthe reaction mixture was purified by HPLC
Sources & evidence
- ORD record
- ord-c5adc629554448f4ad58459475edbddd
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07446199B2
Reaction notes
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