Buchwald–Hartwig amination, record ord-b5c7f8f56eef49a3b7dd9bd1d710bc05
One recorded run of this reaction. Below is what the source recorded, and nothing added to it.
What was in the flask
| Role | Species | Formula | Yield |
|---|---|---|---|
| Reactant | 5-Phenyl-2-pyridinamine | C₁₁H₁₀N₂ | |
| Reactant | 3-Bromopyridine | C₅H₄BrN | |
| Reagent | AdBrettPhos Pd G3 45 | C₅₆H₇₄NO₅PPdS | |
| Reagent | 1,8-Diazabicyclo(5.4.0)undec-7-ene | C₉H₁₆N₂ | |
| Solvent | Dimethyl Sulfoxide | C₂H₆OS | |
| Solvent | Dimethyl Sulfoxide | C₂H₆OS | |
| Solvent | Dimethyl Sulfoxide | C₂H₆OS | |
| Solvent | Dimethyl Sulfoxide | C₂H₆OS | |
| Product | 5-phenyl-N-pyridin-3-ylpyridin-2-amine | C₁₆H₁₃N₃ | |
| Product | 3-Bromopyridine | C₅H₄BrN | |
| Product | 5-Phenyl-2-pyridinamine | C₁₁H₁₀N₂ | |
| Product | Biphenyl | C₁₂H₁₀ |
Conditions
- Duration
- 22 hours
Yield
Procedure
Copied from the source record, unedited
The Mosquito was used to combine the source plate solutions by multi-aspiration of 250 nL of each of the four reaction components and then to dose the resulting reaction mixture (1 uL) into a 1536-well plate
The source
This record comes from experimental reaction archive (ord-b5c7f8f56eef49a3b7dd9bd1d710bc05). Open the source and check it against what is on this page.
experimental reaction archive record ord-b5c7f8f56eef49a3b7dd9bd1d710bc05 from dataset "HTE Pd-catalyzed cross-coupling screen" (doi: 10.1126/science.1259203). No atom mapping is provided by the source.
How to read this record
This is one experiment, not a rule. It says that on one occasion these species were combined under these conditions and this came out. It does not say the reaction will give the same result on your substrate, and nothing on the page has been generalised into a claim that it would.
The pathway is a separate question, kept on separate pages. A mechanism here is the canonical arrow pushing for a class, run on real structures and labelled rule-derived. It is not evidence, and this record is not a mechanism.