HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Toluidine → HCID 68205817, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Toluidine | HCID 7934 | — |
| Reactant | 3-Chloro-N-(propan-2-yl)pyrazin-2-amine | HCID 21477637 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Binap, (A+-)- | HCID 634876 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68205817 | HCID 68205817 | 87.3% |
Reaction Steps
3-chloro-N-isopropylpyrazin-2-amine (6 g, 35.0 mmol), m-toluidine (5.62 g, 52.4 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (0.435 g, 0.699 mmol), Pd2(dba)3 (0.320 g, 0.350 mmol), and sodium t-butoxide (5.04 g, 52.4 mmol) were mixed in 200 mL of toluene and degassed for 20 minutes. The mixture was heated to reflux for 5 h. The reaction was cooled to room temperature and water was added. The reaction mixture was extracted with dichloromethane and washed with water. The crude was columned with 10% ethyl acetate and dichloromethane to give N2-isopropyl-N3-(m-tolyl)pyrazine-2,3-diamine (7.4 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883322B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-7b43fcefbd064fe48b84b75d106b9eab |
| Source note | uspto-grants-2014_11 |