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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 32344Erstellt: 24. Oktober 2026

Pyridine → 2-Anilino-4-[1-isopropyl-2-(methoxyiminomethyl)imidazol-5-yl]pyrimidine

https://huagongshe.com/de/reaction/32344

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktO-Methylhydroxylamine hydrochlorideHCID 521874—
Edukt2-Anilino4-(2-formyl-1-isopropylimidazol-5-yl)pyrimidineHCID 11638102—
LösungsmittelEthanolHCID 702—
Produkt2-Anilino-4-[1-isopropyl-2-(methoxyiminomethyl)imidazol-5-yl]pyrimidineHCID 8676072691%

Reaktionsschritte

Methoxylamine hydrochloride (340 mg, 4.07 mmol) and pyridine (322 mg, 4.07 mmol) was added to a solution of 2-anilino-4-(2-formyl-1-isopropylimidazol-5-yl)pyrimidine (Example 10; 250 mg, 0.814 mmol) in EtOH (10 ml) and the mixture was stirred at ambient temperature for 18 hours. The volatiles were removed by evaporation and the residue triturated with water. The solid product was collected by filtration and dried at 50° C. under vacuum to give the title compound (248 mg, 91%) as a white crystalline solid. NMR (CDCl3): 1.54 (d, 6H), 4.07 (s, 3H), 5.65-5.80 (sept, 1H), 6.95 (d, 1H), 7.15 (m, 2H), 7.34 (t, 2H), 7.50 (s 1H), 7.57 (d, 2H), 8.28 (s, 1H), 8.41 (d, 1 H); m/z 337.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07427626B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-1abed8ef4cef491fbb24b1d7b8cc1856
Quellennotizuspto-grants-2008_09