Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2,5-Dichloropyrimidine | HCID 590641 | — |
| Reactant | Tert-butyl 2-(4-amino-3-fluorophenyl)morpholine-4-carboxylate | HCID 68325450 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86671398 | HCID 86671398 | 31.4% |
Reaction Steps
(RS)-2-(4-Amino-3-fluoro-phenyl)-morpholine-4-carboxylic acid tert-butyl ester (60 mg), 2,5-dichloropyrimidine (30.2 mg, CAS 22536-67-0) and cesium carbonate (99 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 (7.03 mg) and tris(dibenzylideneacetone)dipalladium chloroform complex (6.29 mg) were then added. The reaction mixture was then capped and stirred at 120° C. for 2 hours. 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-chloropyrimidin-2-ylamino)-3-fluorophenyl)morpholine-4-carboxylate (26 mg, 31%) as a colourless amorphous solid. MS (ISP): 411.3 ([{37Cl}M+H]+), 409.2 ([{35Cl}M+H]+), 355.3 ([{37Cl}M+H—C4H8]+), 353.3 ([{35Cl}M+H—C4H8]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802673B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-ea71473424d0463ba04a989b74c998cd |
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| Source note | uspto-grants-2014_08 |
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