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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 75908Erstellt: 25. Oktober 2026

Diisopropylethylamine → AZ-960

https://huagongshe.com/reaction/75908

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt(S)-1-(4-Fluorophenyl)-ethylamineHCID 2779063—
Edukt(S)-5-Chloro-N6-(5-cyclopropyl-1H-pyrazol-3-yl)-N2-(1-(4-fluorophenyl)ethyl)pyridine-2,3,6-triamineHCID 68522447—
Lösungsmittel1-ButanolHCID 263—
LösungsmittelWaterHCID 962—
ProduktAZ-960HCID 2509918491%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

A suspension of 2,5-difluoro-6-(5-methyl-1H-pyrazol-3-ylamino)nicotinonitrile (Method 41, 0.20 g, 0.85 mmol), DIEA (0.14 g, 1.1 mmol), and (S)-1-(4-fluorophenyl)ethanamine (0.23 g, 1.7 mmol) in n-BuOH (2 ml) was heated to 130° C. for 18 hours. The reaction was then cooled to room temperature, diluted with water (20 ml), and extracted with DCM (2×50 ml). The combined organic fractions were dried over Na2SO4, filtered, and then concentrated. The resulting oil was purified by column chromatography (DCM-MeOH=100:1) to give the title compound (0.27 g, 91%). 1H NMR (400 MHz, CD3OD) δ 7.38-7.32 (m, 3H), 7.03-6.99 (m, 2H), 5.99 (br s, 1H), 5.15-5.14 (m, 1H), 2.24 (s, 3H), 1.53 (d, J=6.8 Hz, 3H). MS: Calcd.: 354. Found: [M+H]+ 355.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835465B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-b8c9e5db3a2648b28c3e65b067b4bb83
Quellennotizuspto-grants-2014_09