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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19512Erstellt: 25. Oktober 2026

2-Amino-4-chloro-6-methylpyrimidine → 3-(2-Amino-6-methyl-pyrimidin-4-ylamino)-N-(4-amino-2-methyl-quinolin-6-yl)-propionamide

https://huagongshe.com/reaction/19512

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-4-chloro-6-methylpyrimidineHCID 21810—
EduktDiisopropylethylamineHCID 81531—
Edukt3-Amino-N-(4-amino-2-methyl-quinolin-6-yl)-propionamideHCID 17864629—
LösungsmittelDimethylacetamideHCID 31374—
Produkt3-(2-Amino-6-methyl-pyrimidin-4-ylamino)-N-(4-amino-2-methyl-quinolin-6-yl)-propionamideHCID 1038330936,6%

Reaktionsschritte

A solution of 0.05 g (0.35 mmol) 2-amino-4-chloro-6-methylpyrimidine, 0.204 mg (0.35 mmol) 3-amino-N-(4-amino-2-methyl-quinolin-6-yl)-propionamide and 0.18 mg (1.39 mmol) diisopropyl ethylamine in 5 ml dimethylacetamide was stirred at 100° C. for 2 h. After evaporation of the solvent the residue was purified by HPLC and lyophilized to yield 45 mg of the title compound. MS 352.3 (M+H)+, 1H-NMR (DMSO-d6) δ 2.20 (s, 3H), 2.55 (s, 3H), 2.70 (m, 2H), 3.65 (m, 2H), 6.1 (s, NH), 7.70-7.90 (m, 5H), 8.60-8.80 (br.s., NH), 13.85 (br.s., NH).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745443B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-77ce5778b13d4092b72f4efbd2e07368
Quellennotizuspto-grants-2010_06