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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1522487Erstellt: 25. Oktober 2026

1-Isopropyl-3-methyl-1H-pyrazol-5-amine → Ethyl 3-methyl-1-(1-methylethyl)-6-(4-pyridinyl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylate

https://huagongshe.com/reaction/1522487

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Isopropyl-3-methyl-1H-pyrazol-5-amineHCID 121018—
EduktEthyl 2,4-dioxo-4-(pyridin-4-yl)butanoateHCID 23005473—
LösungsmittelBenzeneHCID 241—
ProduktEthyl 3-methyl-1-(1-methylethyl)-6-(4-pyridinyl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylateHCID 67124410—

Reaktionsschritte

The title compound was prepared in the same manner as described for intermediate 64 using ethyl 2,4-dioxo-4-(4-pyridinyl)butanoate (766 mg, 2.87 mmol), benzene (6 mL), and 3-methyl-1-(1-methylethyl)-1H-pyrazol-5-amine (400 mg, 2.87 mmol). The crude product was purified using column chromatography (Silica gel, eluent: 0 to 30% MeOH/DCM) to give 95 mg (10%) of product. LCMS E-S (M+H)=325.3. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.48-1.56 (m, 3 H), 1.61-1.73 (m, 6 H), 2.77 (s, 3 H), 4.56 (q, J=7.2 Hz, 2 H), 5.37-5.50 (m, 1 H), 8.02-8.16 (m, 3 H), 8.76-8.83 (m, 2 H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09073924B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-a056193faa7343a099097c1f21fdb7a6
Quellennotizuspto-grants-2015_07