Trifluoroacetic acid → HCID 118290350, compound
Reaction equation
C(OC([N:8]1[C:12]([C:13]2[C:14]([NH2:44])=[N:15][CH:16]=[N:17][C:18]=2[N:19]2[CH2:24][CH2:23][CH:22]([C:25]3[N:26]([CH2:38][CH2:39][N:40]4[CH2:43][CH2:42][CH2:41]4)[CH:27]=[C:28]([C:30]4[CH:35]=[CH:34][C:33]([F:36])=[C:32]([CH3:37])[CH:31]=4)[N:29]=3)[CH2:21][CH2:20]2)=[CH:11][CH:10]=[N:9]1)=O)(C)(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[N:40]1([CH2:39][CH2:38][N:26]2[CH:27]=[C:28]([C:30]3[CH:35]=[CH:34][C:33]([F:36])=[C:32]([CH3:37])[CH:31]=3)[N:29]=[C:25]2[CH:22]2[CH2:21][CH2:20][N:19]([C:18]3[N:17]=[CH:16][N:15]=[C:14]([NH2:44])[C:13]=3[C:12]3[NH:8][N:9]=[CH:10][CH:11]=3)[CH2:24][CH2:23]2)[CH2:43][CH2:42][CH2:41]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 5-(4-amino-6-{4-[1-(2-azetidin-1-yl-ethyl)-4-(4-fluoro-3-methyl-phenyl)-1H-imidazol-2-yl]-piperidin-1-yl}-pyrimidin-5-yl)-pyrazole-1-carboxylic acid tert-butyl ester (1.00 eq.) in DCM (1 ml), was added trifluoro-acetic acid (0.5 ml). The reaction mixture was stirred at RT for 30 min. After removal of the solvent, the crude was purified by HPLC to yield the title compound. LC-MS (M+H=502, obsd=502).
Workup
- customAfter removal of the solvent
- customthe crude was purified by HPLC
Sources & evidence
- ORD record
- ord-d2ac954e01b943c987a2a3d3692de65e
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09434714B2
Reaction notes
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