Piperidine → HCID 178426457, compound
Reaction equation
C1CCNCC1.Cc1cc(C#N)cc(C)c1Oc1nc(Nc2ccc(C#N)cc2)nc(N)c1Br>CS(C)=O.O=C(O)C(=O)Nc1cc(C(F)(F)F)cc(C(F)(F)F)c1.O=P([O-])([O-])[O-].[Cu][I].[K+].[K+].[K+]>Cc1cc(C#N)cc(C)c1Oc1nc(Nc2ccc(C#N)cc2)nc(N)c1N1CCCCC1Participants
7
Reactant 2
Product 1
Reagents, catalysts & solvents 4
Conditions
- Temperature
- 80 °C
Workup
- additionThe reaction vials were then cooled to r.t. and diluted with 100 μL of 5% AcOH in DMSO, containing 1,3,5-trimethoxybenzene (0.005M) and were shaken vigorously.
- aliquot25 microliter of resulting solution is taken
- additionTo the 25 microliter aliquot 700 microliter of MeCN was added prior to UPLC-MS Analysis
Sources & evidence
- ORD record
- ord-e74c70aae3f845fd9b4800faef593473
- Source dataset
- Figure 4 from Chemistry informer libraries
- Original link
- View source
Reaction notes
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