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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 605906Erstellt: 25. Oktober 2026

Diisopropylethylamine → (5-Bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-(3-fluoro-4-morpholin-4-yl-phenyl)-amine

https://huagongshe.com/reaction/605906

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt3-Fluoro-4-morpholinoanilineHCID 1485330—
Edukt5,8-Dibromo-(1,2,4)triazolo(1,5-a)pyrazineHCID 49758022—
Edukt4-{8-[4-(4-Methyl-piperazin-1-yl)-phenylamino]-[1,2,4]triazolo[1,5-a]pyrazin-5-yl}-thiophene-2-carboxylic acid amideHCID 57589928—
LösungsmittelIsopropanolHCID 3776—
Produkt(5-Bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-(3-fluoro-4-morpholin-4-yl-phenyl)-amineHCID 5758999798,5%

Reaktionsschritte

This compound may be prepared using methods as described for Compound 6, step 1 using 5,8-dibromo-[1,2,4]triazolo[1,5-a]pyrazine (0.5 g, 1.799 mmol), 3-fluoro-4-morpholin-4-yl-phenylamine (0.53 g, 2.70 mmol), and DIPEA (0.470 mL, 2.70 mmol) in 2-propanol (6 mL). The reaction mixture is partitioned between 10% citric acid aqueous solution and DCM. The organic phase is separated and washed with water and brine, dried over MgSO4, filtered and concentrated under vacuum to afford the title compound (697 mg, 98%) which is used in the next step without further purification. LCMS: Rt 3.52 min (98.2%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07915256B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-27112b23025d4d1797f595b435c6a5de
Quellennotizuspto-grants-2011_03