HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240366Generated: October 28, 2026
2-Amino-6-methylpyridine → HCID 86643866, compound
https://huagongshe.com/reaction/240366
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Amino-6-methylpyridine | HCID 15765 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | HCID 17861074 | HCID 17861074 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86643866 | HCID 86643866 | 105.3% |
Reaction Steps
37.8 g (0.11 mol) of 2-bromo-N-(diphenylmethylene)aniline was dissolved in toluene (100 ml), and 14.6 g (0.13 mol) of 2-amino-6-picoline, 5.2 g (5.5 mmol) of tris(dibenzylideneacetone)dipalladium(0), 11.2 g (17.6 mmol) of 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl, and 15.2 g (0.15 mol) of sodium-t-butoxide were added thereto. The mixture was stirred for 2 hours at 100° C. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was washed with methanol to obtain 42.1 g (yield:>99%) of N1-(diphenylmethylene)-N2-(6-methylpyridine-2-yl)benzene-1,2-diamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08648075B2 |
|---|
| Source dataset | uspto-grants-2014_02 |
|---|
| ORD ID | ord-d6db223438174159aca2e4548efc383a |
|---|
| Source note | uspto-grants-2014_02 |
|---|