HCID 58446794, compound → 4-(3-Fluoro-azetidine-1-carbonyl)-2-methyl-2H-pyrazole-3-carboxylic acid {2-[3-(2-fluoro-ethoxy)-phenyl]imidazo[1,2-a]pyrimidin-7-yl}-amide
Reaction equation
[F:1][CH2:2][CH2:3][O:4][C:5]1[CH:6]=[C:7]([C:11]2[N:12]=[C:13]3[N:18]=[C:17]([NH2:19])[CH:16]=[CH:15][N:14]3[CH:20]=2)[CH:8]=[CH:9][CH:10]=1.[F:21][CH:22]1[CH2:25][N:24]([C:26]([C:28]2[CH:29]=[N:30][N:31]([CH3:36])[C:32]=2[C:33](O)=[O:34])=[O:27])[CH2:23]1>>[F:1][CH2:2][CH2:3][O:4][C:5]1[CH:6]=[C:7]([C:11]2[N:12]=[C:13]3[N:18]=[C:17]([NH:19][C:33]([C:32]4[N:31]([CH3:36])[N:30]=[CH:29][C:28]=4[C:26]([N:24]4[CH2:23][CH:22]([F:21])[CH2:25]4)=[O:27])=[O:34])[CH:16]=[CH:15][N:14]3[CH:20]=2)[CH:8]=[CH:9][CH:10]=1Participants
3
Procedure
The title compound was prepared in analogy to example 82 from 2-(3-(2-fluoroethoxy)phenyl)imidazo[1,2-a]pyrimidin-7-amine (120 mg) and 4-(3-fluoroazetidine-1-carbonyl)-1-methyl-1H-pyrazole-5-carboxylic acid (100 mg, 440 μmol). Light brown solid (132 mg, 60%). MS (m/z)=482.2 [M+H+].
Sources & evidence
- ORD record
- ord-f9de7b8e908c4c24b70c012b128b88c0
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08410117B2
Reaction notes
Loading…