p-Toluidine → 2-Pyridinamine, N-(4-methylphenyl)-

HRID 739647Notes

Reaction equation

HRID 739647 reaction equation
Brc1ccccn1.Cc1ccc(N)cc1>CC(C)c1cc(C(C)C)c(-c2ccccc2[P](C(C)(C)C)(C(C)(C)C)->[Pd]2(<-[NH2]c3ccccc3-c3cccc[c]32)[O]S(=O)(=O)C(F)(F)F)c(C(C)C)c1.CCN=P(N=P(N(C)C)(N(C)C)N(C)C)(N(C)C)N(C)C.CCOC(=O)c1cnoc1.CS(C)=O>Cc1ccc(Nc2ccccn2)cc1

Participants

7

Reactant 2

HCID 7813p-ToluidineHCID 79732-Bromopyridine

Product 1

HCID 27864192-Pyridinamine, N-(4-methylphenyl)-Yield 4.841%

Reagents, catalysts & solvents 4

HCID 33931062,N'3,N'3,N3,N3,N'5,N'5,N5,N5-nonamethyl-2,4,6-triaza-3lambda5,5lambda5-diphosphaocta-3,5-diene-3,3,5,5-tetramineReagentHCID 15590757Ethyl 1,2-oxazole-4-carboxylateReagentHCID 178439023HCID 178439023, compoundCatalystHCID 679Dimethyl SulfoxideSolvent5×

Conditions

Temperature
60 °C

Procedure

These solutions were added to a 384- well source plate (80 µL per well). The Mosquito HTS liquid handling robot was used to dose each of these solutions (200 nL each) into a 1536-well plate.

Workup

  1. additionNo procedure recorded

Sources & evidence

ORD record
ord-0946f7f8e5a445eeac5233f2f2706e5b
Source dataset
Ahneman

Reaction notes

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