Piperidine → HCID 178525856, compound

HRID 1652132Notes

Reaction equation

HRID 1652132 reaction equation
C1CCNCC1.O=C(O)Cn1nnc(-c2cc(N3CCC(Oc4cc(F)ccc4Br)CC3)no2)n1>C1CN2CCN1CC2.CC(C)(C)c1ccnc(-c2cc(C(C)(C)C)ccn2)c1.COCCOC.CS(C)=O.F[P-](F)(F)(F)(F)F.[Cl][Ni][Cl].c1ccc(-c2cccc[c]2[Ir+][c]2ccccc2-c2ccccn2)nc1>O=C(O)Cn1nnc(-c2cc(N3CCC(Oc4cc(F)ccc4N4CCCCC4)CC3)no2)n1

Participants

7

Reactant 2

HCID 8082PiperidineHCID 24988881Mk-8245

Product 1

HCID 178525856HCID 178525856, compoundYield 0%

Reagents, catalysts & solvents 4

HCID 9237DabcoCatalystHCID 15773433Dichloronickel;1,2-dimethoxyethaneCatalystHCID 178441140HCID 178441140, compoundCatalystHCID 679Dimethyl SulfoxideSolvent3×

Conditions

Temperature
55 °C

Workup

  1. 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
  2. aliquot25 microliter of quenched reaction mixture was taken
  3. 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-9232bfc784af4110806708606993c735
Source dataset
Nano CN PhotoChemistry Informers Library
Original link
View source

Reaction notes

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