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HRID 11831Erstellt: 25. Oktober 2026

1H-Pyrazol-3-amine, 5-methyl- → HCID 178419098, Verbindung

https://huagongshe.com/reaction/11831

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1H-Pyrazol-3-amine, 5-methyl-HCID 93146—
Edukt4-Chloro-2-phenylpyrido[2,3-D]pyrimidineHCID 12203870—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178419098HCID 17841909850,7%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

To a solution of 4-chloro-2-phenyl-pyrido[2,3-d]pyrimidine (J. Pharm. Belg., 29, 1974, 145–148) (109 mg, 0.45 mmol) in THF (15 mL) was added 3-amino-5-methyl pyrazole (48 mg, 0.5 mmol) and the resulting mixture heated at 65° C. overnight. The mixture was cooled to room temperature and the resulting suspension was filtered and washed with Et2O. The solid was dissolved in a mixture EtOH:water and the pH adjusted to pH 7. The aqueous was extracted twice with ethyl acetate and the combined organic layers were dried (MgSO4), filtered, and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, DCM-MeOH gradient) to afford IV-31 as an off-white solid (69 mg, 50%): mp 234° C.; 1H NMR (DMSO) δ 2.14 (3H, s), 5.99 (1H, s), 7.20–7.40 (3H, m), 7.40–7.50 (3H, m), 8.60 (1H, d), 8.79 (1H, d), 12.82 (1H, br s); IR (solid) 2957, 2921, 2857, 1644, 1560, 1459, 1427; MS 303.2 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098330B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-74bd5f909fdd45cab060be5e2f1707cd
Quellennotizuspto-grants-2006_08