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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1725589Erstellt: 27. Oktober 2026

Water → (5-Fluoro-1H-indazol-3-yl)-[6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidin-4-yl]amine

https://huagongshe.com/reaction/1725589

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium BicarbonateHCID 516892—
Edukt5-fluoro-1H-indazol-3-amineHCID 4327896—
Edukt4-Chloro-6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidineHCID 21939271—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt(5-Fluoro-1H-indazol-3-yl)-[6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidin-4-yl]amineHCID 1038552256,5%

Reaktionsbedingungen

Temperatur165 °C

Reaktionsschritte

A mixture of 4-chloro-6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidine (0.10 g, 0.37 mmol) and 5-fluoro-1H-indazole-3-ylamine (0.072 g, 0.48 mmol) was heated neat at 160-170° C. for 8 hours. The resulting residue was cooled to ambient temperature then dissolved in N-methyl-pyrrolidinone (2 mL). This mixture was poured into water (20 mL) and sodium bicarbonate (5 mL) was added and the resulting mixture filtered, washing with water. Purification by preparative HPLC provided the title compound (0.081 g, 43% yield) as a tan solid. 1H-NMR (500 MHz, DMSO-d6) δ 12.8 (br s, 1H), 10.6 (br s, 1H), 7.86 (d, J=8.0 Hz, 1H), 7.77 (m, 4H), 7.62 (br s, 1H), 7.50 (m, 1H), 7.29 (m, 1H), 2.44 (s, 3H) ppm; LC-MS 388.05 (M+H); Rt (Method A) 2.900 minutes.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07491730B2
Quelldatensatzuspto-grants-2009_02
ORD IDord-c3208dd52f5a409da9fa3114d393fd99
Quellennotizuspto-grants-2009_02