Diethyl (4-{[4-{[4-bromo-2-(methylcarbamoyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-2-yl]amino}benzyl)phosphonate → Diethyl(4-{[4-{[4-{1-[2-(diethylamino)ethyl]-1H-pyrazol-4-yl}-2-(methylcarbamoyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-2-yl]amino}benzyl)phosphonate
Reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[C:14]([C:15]([F:18])([F:17])[F:16])=[CH:13][N:12]=[C:11]([NH:19][C:20]3[CH:34]=[CH:33][C:23]([CH2:24][P:25](=[O:32])([O:29][CH2:30][CH3:31])[O:26][CH2:27][CH3:28])=[CH:22][CH:21]=3)[N:10]=2)=[C:4]([C:35](=[O:38])[NH:36][CH3:37])[CH:3]=1.[CH2:39]([N:41]([CH2:58][CH3:59])[CH2:42][CH2:43][N:44]1[CH:48]=[C:47](B2OC(C)(C)C(C)(C)O2)[CH:46]=[N:45]1)[CH3:40]>>[CH2:27]([O:26][P:25]([CH2:24][C:23]1[CH:33]=[CH:34][C:20]([NH:19][C:11]2[N:10]=[C:9]([NH:8][C:5]3[CH:6]=[CH:7][C:2]([C:47]4[CH:46]=[N:45][N:44]([CH2:43][CH2:42][N:41]([CH2:58][CH3:59])[CH2:39][CH3:40])[CH:48]=4)=[CH:3][C:4]=3[C:35](=[O:38])[NH:36][CH3:37])[C:14]([C:15]([F:18])([F:17])[F:16])=[CH:13][N:12]=2)=[CH:21][CH:22]=1)(=[O:32])[O:29][CH2:30][CH3:31])[CH3:28]Participants
3
Reactant 2
Product 1
Procedure
The title compound was prepared according to the procedure of Example 97 using Diethyl(4-{[4-{[4-bromo-2-(methylcarbamoyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-2-yl]amino}benzyl)phosphonate (Example 106) and N,N-diethyl-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]ethanamine (Compound 175A). MS (ES+): m/z 703.45 (100) [MH+]; HPLC: tR=0.73 min (UPLC, purity).
Sources & evidence
- ORD record
- ord-7e989475bf5e427591774e51904eec86
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08399433B2
Reaction notes
Loading…