HCID 49758770, compound → Biphenyl

HRID 609350Notes

Reaction equation

HRID 609350 reaction equation
CC1(C)OB(c2cnc(-n3cccn3)nc2)OC1(C)C.CCCc1nc2ccc(I)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1.CN(C)C(=NC(C)(C)C)N(C)C>CC(C)c1cc(C(C)C)c(-c2ccccc2[PH](C(C)(C)C)(C(C)(C)C)[Pd]2([O]S(C)(=O)=O)[NH]c3ccccc3-c3cccc[c]32)c(C(C)C)c1.CS(C)=O.O>CCCc1nc2ccc(-c3cnc(-n4cccn4)nc3)cc2c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1

Participants

9

Reactant 2

HCID 49758770HCID 49758770, compoundHCID 132556033HCID 132556033, compound

Product 3

HCID 7095BiphenylHCID 132556033HCID 132556033, compoundHCID 178439866HCID 178439866, compound

Reagents, catalysts & solvents 4

HCID 178439025HCID 178439025, compoundCatalystHCID 679Dimethyl SulfoxideSolvent4×HCID 962WaterSolventHCID 35715812-tert-Butyl-1,1,3,3-tetramethylguanidineOther

Workup

  1. additionAfter 22 hours the crude reactions were diluted with 3 x 1 uL 0.5 M AcOH in DMSO (containing PhPh as an internal standard). The reactions were mixed after each dispense operation.
  2. aliquotMosquito(R) was used to transfer 1 uL of each quenched reaction from the 1,536-well reaction plate to 384-well analytical plates containing 60 uL DMSO for analysis.

Sources & evidence

ORD record
ord-4f83136243bf45ac9f8613a8480538dc
Source dataset
Cernak miniaturized Suzuki Cross-Coupling 12x10 Informer Library
Original link
View source

Reaction notes

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