Trifluoroacetic acid → HCID 178457734, compound
Reaction equation
[OH:1][C:2]1[C:7]([C:8]([NH:10][C:11]([CH3:20])([C:13]([O:15]C(C)(C)C)=[O:14])[CH3:12])=[O:9])=[CH:6][N:5]=[C:4]([N:21]2[CH:25]=[CH:24][CH:23]=[N:22]2)[N:3]=1.C(O)(C(F)(F)F)=O>C(Cl)Cl>[OH:1][C:2]1[C:7]([C:8]([NH:10][C:11]([CH3:12])([C:13]([OH:15])=[O:14])[CH3:20])=[O:9])=[CH:6][N:5]=[C:4]([N:21]2[CH:25]=[CH:24][CH:23]=[N:22]2)[N:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The product of Step A (3.0 g, 8.64 mmol) was combined with DCM (18 ml) and TFA (2.5 mL). The reaction was aged at reflux for about 5 h and then concentrated. The product was then treated with Et2O, isolated by filtration, and washed with hexane to afford the title compound. HPLC/MS: 292.0 (M+1); Rt=1.42 min.
Workup
- temperatureat reflux for about 5 h
- concentrationconcentrated
- additionThe product was then treated with Et2O
- customisolated by filtration
- washwashed with hexane
Sources & evidence
- ORD record
- ord-1d308b88f7ca4cca9cbe3f515648251e
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08278304B2
Reaction notes
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