Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2111665Erstellt: 25. Oktober 2026

Diisopropylethylamine → 5-Bromo-2-(3-methylisoxazol-5-ylmethylamino)-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidine

https://huagongshe.com/reaction/2111665

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt(3-Methyl-1,2-oxazol-5-yl)methanamine hydrochlorideHCID 45792534—
Edukt5-bromo-2-chloro-N-(5-methyl-1H-pyrazol-3-yl)-4-PyrimidinamineHCID 50993645—
Lösungsmittel1-ButanolHCID 263—
Produkt5-Bromo-2-(3-methylisoxazol-5-ylmethylamino)-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidineHCID 6015428531%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of 5-aminomethyl-3-methylisoxazole hydrochloride (890 mg, 6.0 mmol), 5-bromo-2-chloro-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidine (Method 1; 578 mg, 2.0 mmol) and N,N-diisopropylethylamine (1.4 ml, 8.0 mmol) in 1-butanol (10 ml) was heated at 120° C. for 18 hours. The mixture was allowed to cool to ambient temperature and volatiles removed by evaporation. The residue was triturated with ether and the product collected by filtration to give the titled compound (225 mg, 31%). 1H NMR (DMSO): δ 2.15 (s, 3H), 2.2 (s, 3H), 4.5 (m, 2H), 6.1 (br s, 2H), 7.6 (br s, 1H), 8.0 (br s, 2H), 12.05 (br s, 1H); MS: m/z 366.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07521453B2
Quelldatensatzuspto-grants-2009_04
ORD IDord-cf5dbee485fe4d8dbb0df7bc2ba3b85d
Quellennotizuspto-grants-2009_04