Piperidine → HCID 178439936, compound
Reaction equation
C1CCNCC1.CCCc1nc2ccc(I)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1>C1CN2CCN1CC2.COCCOC.CS(C)=O.FC(F)(F)C1=CC2Sc3ccccc3N(c3ccccc3)C2C=C1.FC(F)(F)c1cc(-c2c3ccccc3[n+](-c3cc(C(F)(F)F)cc(C(F)(F)F)c3)c3ccccc23)cc(C(F)(F)F)c1.[Cl-].[Cl][Ni][Cl]>CCCc1nc2ccc(N3CCCCC3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1Participants
8
Reactant 2
Product 1
Reagents, catalysts & solvents 5
Conditions
- Temperature
- 55 °C
Workup
- additionThe samples was moved from a 1536 well plate into a 384 well plate. The 384 well plate contained 75 microliter of 1% Acetic acid in DMSO solution with 0.003M trimethoxybenzene. The reaction plate was rinsed three times with the same solution to make a total addition volume of ~90 microliters
- aliquot25 microliter of quenched reaction mixture was taken
- additionTo the 25 microliter aliquot 50 microliter of DMSO was added. If the original reaction concentration was 0.05 M (wrt limiting reagent). This would make a final analytical concentration of 0.36 mM which is in line with typical analytical concentrations from this group.
Sources & evidence
- ORD record
- ord-95dde9df75714eaaa968ed6d65398a8d
- Source dataset
- Nano CN PhotoChemistry Informers Library
- Original link
- View source
Reaction notes
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