Piperidine → HCID 178462863, compound
Reaction equation
C1CCNCC1.CCn1c(=O)c2c(nc(N[C@@H]3CCC[C@H]3O)n2Cc2ccc(OC)c(Br)c2)n(CCO)c1=O>COc1cccc(OC)c1NC(=O)C(=O)O.CS(C)=O.O=P([O-])([O-])[O-].[Cu][I].[K+].[K+].[K+]>CCn1c(=O)c2c(nc(N[C@@H]3CCC[C@H]3O)n2Cc2ccc(OC)c(N3CCCCC3)c2)n(CCO)c1=OParticipants
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-1e9819fc13134d6388708454c61c4d78
- Source dataset
- Figure 4 from Chemistry informer libraries
- Original link
- View source
Reaction notes
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