Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Aminopyridine | HCID 10009 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | ((1S,2R)-2-((6-chloro-5-cyanopyrazin-2-yl)amino)cyclohexyl)carbamate | HCID 86685625 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86685627 | HCID 86685627 | 112.4% |
Reaction Steps
The mixture of tert-tutyl ((1S,2R)-2-((6-chloro-5-cyanopyrazin-2-yl)amino)cyclohexyl)carbamate (100 mg, 0.28 mmol), 3-aminopyridine (53 mg, 0.56 mmol), powder cesium carbonate (360 mg, 1.12 mmol), BINAP (37 mg, 0.06 mmol), Pd(OAc)2 (14 mg, 0.06 mmol) in 20 mL dioxane was degassed with argon stream. It was stirred in argon atmosphere at 110° C. for 2 h. The mixture was cooled, diluted with 100 mL EtOAc, vigorously stirred, and filtered through celite. The filtrate was concentrated and subjected to silica flash column with 0-70% EtOAc in hexane to isolate the coupling product. It was then stirred in 6 mL TFA and 1 mL conc. H2SO4 at 80° C. for 30 m. It was cooled in ice bath, diluted with water, filtered, and subjected to reverse phase preparative HPLC to isolate the title compound (103 mg). MS found for C16H21N7O as (M+H)+ 328.5. UV: λ=230, 259, 301 nm. 1H NMR: (CD3OD) δ 9.50 (1H, s), 8.56 (1H, d, J=8.8 Hz), 8.42 (1H, d, J=5.6 Hz), 7.95 (1H, dd, J=8.8; 5.6 Hz), 7.75 (1H, s), 4.57 (1H, m), 3.70 (1H, m), 1.95-1.58 (8H, m) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877760B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-78ff642b3cae45afa657de7196aac1d2 |
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| Source note | uspto-grants-2014_11 |
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