Trifluoroacetic acid → HCID 86605020, compound
Reaction equation
[F:1][C:2]([F:21])([F:20])[C:3]([N:5]1[CH2:10][CH2:9][CH:8]([NH:11][NH:12]C(OC(C)(C)C)=O)[CH2:7][CH2:6]1)=[O:4].[F:22][C:23]([F:28])([F:27])[C:24]([OH:26])=[O:25]>ClCCl>[F:21][C:2]([F:1])([F:20])[C:3]([N:5]1[CH2:10][CH2:9][CH:8]([NH:11][NH2:12])[CH2:7][CH2:6]1)=[O:4].[F:22][C:23]([F:28])([F:27])[C:24]([O-:26])=[O:25]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5.0 g (16.1 mmol) tert-butyl N′-[1-(2,2,2-trifluoro-acetyl)-piperidin-4-yl]-hydrazine-carboxylate are dissolved in 50 ml dichloromethane and combined with 6.0 ml (77.9 mmol) trifluoroacetic acid. The reaction mixture is stirred for 5 hours at ambient temperature, then concentrated by evaporation. Yield: 6.70 g
Workup
- concentrationconcentrated by evaporation
Sources & evidence
- ORD record
- ord-efe3247449b2408ab25f0fd532c5457e
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08232286B2
Reaction notes
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