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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200517Generated: October 27, 2026

Sulfuric Acid → HCID 86685633, compound

https://huagongshe.com/reaction/2200517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactant((1S,2R)-2-((6-chloro-5-cyanopyrazin-2-yl)amino)cyclohexyl)carbamateHCID 86685625—
ReactantHCID 86685631HCID 86685631—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTrifluoroacetic acidHCID 6422—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86685633HCID 8668563358.7%

Reaction Conditions

Temperature110 °C

Reaction Steps

The mixture of tert-tutyl ((1S,2R)-2-((6-chloro-5-cyanopyrazin-2-yl)amino)cyclohexyl)carbamate (60 mg, 0.24 mmol), 3,5-di(pyrimidin-2-yl)aniline (85 mg, 0.24 mmol), powder cesium carbonate (326 mg, 1.00 mmol), BINAP (31 mg, 0.05 mmol), Pd(OAc)2 (12 mg, 0.05 mmol) in 15 mL dioxane was degassed with argon stream. It was stirred in argon atmosphere at 110° C. for 2.5 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 0-90% EtOAc in hexane to isolate the coupling product. It was then stirred in 5 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 (68 mg). MS found for C25H26N10O as (M+H)+483.5. UV: λ=254, 315 nm. 1H NMR: (CD3OD) δ 9.05 (1H, t, J=1.6 Hz), 8.83 (4H, d, J=5.2 Hz), 8.75 (2H, d, J=1.6 Hz), 7.48 (1H, s), 7.35 (2H, t, J=4.8 Hz), 4.71 (1H, m), 3.60 (1H, m), 1.82-1.39 (8H, m) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359308B2
Source datasetuspto-grants-2016_06
ORD IDord-5192ca502f9c49afa794cc6eb488249b
Source noteuspto-grants-2016_06