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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 449905Erstellt: 24. Oktober 2026

Cesium carbonate → 2,6-dichloro-4-cyano-N-(2-(2,6-dimethylpyrimidin-4-ylamino)-3-nitropyridin-4-yl)benzamide

https://huagongshe.com/de/reaction/449905

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt2,6-Dimethyl-4-aminopyrimidineHCID 68039—
Edukt1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
EduktN-(2-chloro-3-nitropyridin-4-yl)-2,6-dichloro-4-cyanobenzamideHCID 86648955—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2,6-dichloro-4-cyano-N-(2-(2,6-dimethylpyrimidin-4-ylamino)-3-nitropyridin-4-yl)benzamideHCID 596184065%

Reaktionsschritte

A 25 mL microwave tube containing N-(2-chloro-3-nitropyridin-4-yl)-2,6-dichloro-4-cyanobenzamide (100 mg, 0.27 mmol), 2,6-dimethylpyrimidin-4-amine (43 mg, 0.35 mmol), Pd2(dba)3 (8 mg, 0.009 mmol), Cs2CO3 (180 mg, 0.54 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (Xantphos, 4 mg, 0.005 mmol), dioxane (8 mL) and DME (3 mL) was degassed and then charged by N2 (3×). The mixture was then irradiated in a microwave reactor at 160° C. for 2 hours and then diluted with dioxane (20 mL). The reaction was filtered through Celite and concentrated under reduced pressure. The residue was purified by reverse-phase HPLC (Gemini, 200 mm×25 mm, gradient: CH3CN/0.05% NH3.H2O, 50-80, 10 min) to afford the desired product (4 mg, yield: 5%). LCMS (ESI) m/z: 458.3 [M+H+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08486950B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-650efcb8aa104dc69f9c83da8e541b8c
Quellennotizuspto-grants-2013_07