Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200518Generated: October 29, 2026

Sulfuric Acid → HCID 71571949, compound

https://huagongshe.com/reaction/2200518

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 C21H24N12O 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 numberUS09359308B2
Source datasetuspto-grants-2016_06
ORD IDord-c1a924f67bbe4c249cc695b80cda43a1
Source noteuspto-grants-2016_06