Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Reactant | HCID 68325506 | HCID 68325506 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68327931 | HCID 68327931 | 44% |
Reaction Steps
tert-butyl (RS)-2-(4-amino-3-methylphenyl)morpholine-4-carboxylate (60 mg), 2,5-dibromopyridine (48.6 mg, CAS 624-28-2) and cesium carbonate (100 mg) were combined with dioxane (2 ml) to give a yellow suspension. The mixture was degassed by bubbling argon into the mixture for several minutes. Xantphos (7.12 mg) and tris(dibenzylideneacetone)dipalladium chloroform complex (6.37 mg) were then added. The reaction mixture was then capped and stirred at 80° C. for 1 hour. The crude reaction mixture was cooled to room temperature and filtered. The filtrate was concentrated in vacuo and the residue was purified by flash column chromatography (silica gel; gradient: 0% to 80% EtOAc in hexanes) to afford tert-butyl (RS)-2-(4-(5-bromopyridin-2-ylamino)-3-methylphenyl)morpholine-4-carboxylate (40 mg, 44%) as a colourless amorphous solid. MS (ISP): 450.2 ([{81Br}M+H]+), 448.1 ([{79Br}M+H]+), 394.3 ([{81Br}M+H—C4H8]+), 392.1 ([{79Br}M+H—C4H8]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08802673B2 |
|---|
| Source dataset | uspto-grants-2014_08 |
|---|
| ORD ID | ord-ed793cb1f9c947f8ba918412e13ab69c |
|---|
| Source note | uspto-grants-2014_08 |
|---|