Trifluoroacetic acid → HCID 178511076, compound
Reaction equation
[C:1]([CH2:3][C@H:4]1[CH2:9][CH2:8][C@H:7]([CH2:10][NH:11]C(=O)OC(C)(C)C)[CH2:6][CH2:5]1)#[N:2].FC(F)(F)C(O)=O>ClCCl>[NH2:11][CH2:10][C@H:7]1[CH2:8][CH2:9][C@H:4]([CH2:3][C:1]#[N:2])[CH2:5][CH2:6]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of tert-butyl (trans-4-(cyanomethyl)cyclohexyl)methylcarbamate (500 mg) in dichloromethane (5 mL) was slowly added trifluoroacetic acid (3 mL) at 0° C. The mixture was warmed to room temperature, stirred for 1 hour and concentrated. The residue was dried under vacuum to provide the title compound.
Workup
- customat 0° C
- concentrationconcentrated
- customThe residue was dried under vacuum
Sources & evidence
- ORD record
- ord-eaecf07e76bc48aab610871b166e2983
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08952157B2
Reaction notes
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