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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 332837Erstellt: 24. Oktober 2026

Sulfuric Acid → HCID 86685628, Verbindung

https://huagongshe.com/de/reaction/332837

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktCesium carbonateHCID 10796—
Edukt5-Fluoro-3-pyridinamineHCID 574450—
EduktBinap, (A+-)-HCID 634876—
EduktHCID 86685625HCID 86685625—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelTrifluoroacetic acidHCID 6422—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktHCID 86685628HCID 8668562885,8%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08877760B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-29df8ee851fc429f83591399850729bf
Quellennotizuspto-grants-2014_11