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HRID 1272761Erstellt: 25. Oktober 2026

3-Pyridinemethanamine → N5-(3-Pyridylmethyl)-3-(4-fluorophenyl)-1H-5-indazolecarboxamide

https://huagongshe.com/reaction/1272761

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-PyridinemethanamineHCID 31018—
Edukt1-acetyl-3-(4-fluorophenyl)-1H-indazole-5-carbonyl chlorideHCID 22480227—
LösungsmittelPyridineHCID 1049—
ProduktN5-(3-Pyridylmethyl)-3-(4-fluorophenyl)-1H-5-indazolecarboxamideHCID 2226070041%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a flask containing 1-acetyl-3-(4-fluorophenyl)-1H-indazole-5-carbonyl chloride (300 mg, 0.95 mmol) dissolved in pyridine (4 mL) was added 3-aminomethyl pyridine (106 μl, 1.05 mmol). The reaction was allowed to stir under a nitrogen atmosphere overnight. LCMS indicated the reaction was complete. Solvent was removed and water was added to the flask. A solid crashed out of solution that was collected by filtration. The solid was taken up in a 3% ammonia in methanol solution (8 mL) and allowed to reflux at 60° C. for three hours. The reaction was neutralized with 1 N HCl solution and extracted with ethyl acetate. The organic layer was dried with magnesium sulfate, filtered and concentrated to yield the title compound (134 mg, 41% yield). 1H NMR (DMSO-d6) δ 13.5 (s, 1H), 9.2 (s, 1H), 8.6 (m, 2H), 8.5 (s, 1H), 8.1 (m, 2H), 7.95 (d, 1H), 7.65 (d, 1H), 7.6 (m, 1H), 7.4 (m, 3H), 4.6 (m, 2H) ES-MS m/z 347 [M+1]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07208513B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-a96b3c0d58724fa1b1c681c462bc9ab8
Quellennotizuspto-grants-2007_04