HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432109Generated: October 25, 2026
Oxygen → Tert-butyl 2-(but-3-enylamino)-6-methylisonicotinate
https://huagongshe.com/reaction/1432109
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | 3-Buten-1-amine | HCID 443732 | — |
| Reactant | 2-Chloro-6-methyl-isonicotinic acid tert-butyl ester | HCID 86040366 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl 2-(but-3-enylamino)-6-methylisonicotinate | HCID 68545468 | — |
Reaction Steps
Under rigorous exclusion of oxygen a mixture of 200 mg (0.88 mmol) 2-chloro-6-methyl-isonicotinic acid tert-butyl ester, 10 mg palladium(II)acetate (0.044 mmol), 27 mg (0.44 mol) BINAP (R(+)-2,2-bis(diphenylphosphino)-1,1-binaphtalene) and 62 mg (0.88 mmol) but-3-enylamine in 10 ml toluene is heated at 60° C. for 4 h. The mixture is diluted with EtOAc, washed with 10% aqueous NaHCO3 and water, dried with sodium sulfate and evaporated. Chromatography of the product on silica gel (hexane/EtOAc 9:1) yields the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07612055B2 |
|---|
| Source dataset | uspto-grants-2009_11 |
|---|
| ORD ID | ord-d15b92506bb348ecaa7e92541511aab2 |
|---|
| Source note | uspto-grants-2009_11 |
|---|