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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200512Generated: October 26, 2026

Sulfuric Acid → 5-(((1R,2S)-2-aminocyclohexyl)amino)-3-((5-fluoropyridin-3-yl)amino)pyrazine-2-carboxamide

https://huagongshe.com/reaction/2200512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantCesium carbonateHCID 10796—
Reactant5-Fluoro-3-pyridinamineHCID 574450—
ReactantBinap, (A+-)-HCID 634876—
ReactantHCID 86685625HCID 86685625—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTrifluoroacetic acidHCID 6422—
Solvent1,4-DioxaneHCID 31275—
Product5-(((1R,2S)-2-aminocyclohexyl)amino)-3-((5-fluoropyridin-3-yl)amino)pyrazine-2-carboxamideHCID 8668562885.8%

Reaction Conditions

Temperature110 °C

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-fluoro-5-aminopyridine (60 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 0-60% 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 (83 mg). MS found for C16H20FN7O as (M+H)+346.5. UV: λ=259, 301 nm. 1H NMR: (CD3OD) δ 9.04 (1H, m), 8.57 (1H, m), 8.40 (1H, m), 7.73 (1H, s), 4.49 (1H, m), 3.74 (1H, m), 1.96-1.60 (8H, m) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359308B2
Source datasetuspto-grants-2016_06
ORD IDord-54e0cc3f646c4348ac59adc8d5c75bb4
Source noteuspto-grants-2016_06