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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332844Generated: October 27, 2026

Sulfuric Acid → HCID 71571949, compound

https://huagongshe.com/reaction/332844

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 86685634HCID 86685634—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTrifluoroacetic acidHCID 6422—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 71571949HCID 7157194915%

Reaction Conditions

Temperature110 °C

Reaction Steps

The mixture of tert-tutyl ((1S,2R)-2-((6-chloro-5-cyanopyrazin-2-yl)amino)cyclohexyl)carbamate (90 mg, 0.26 mmol), 3,5-di(2H-1,2,3-triazol-2-yl)aniline (88 mg, 0.39 mmol), powder cesium carbonate (340 mg, 1.04 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 16 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 0-55% 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 20 m. It was cooled in ice bath, diluted with water, filtered, and subjected to reverse phase preparative HPLC to isolate the title compound (18 mg). MS found for C21H24N120 as (M+H)+ 461.5. UV: λ=259, 311 nm. 1H NMR: (CD3OD) δ 8.52 (2H, d, J=1.6 Hz), 8.43 (1H, t, J=1.6 Hz), 8.01 (4H, s), 7.61 (2H, s), 4.83 (1H, m), 3.76 (1H, m), 1.93-1.55 (8H, m) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877760B2
Source datasetuspto-grants-2014_11
ORD IDord-409913fc08824c00ad21c5111bc44414
Source noteuspto-grants-2014_11