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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 253703Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/253703

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
PatentnummerUS07872129B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-9502545c17784914b5a2cfe4a1d4e8bc
Quellennotizuspto-grants-2011_01