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HRID 60198Erstellt: 24. Oktober 2026

4-(Trifluoromethyl)aniline → [2-(2,6-Dichloro-benzyl)-oxazolo[5,4-d]pyrimidin-7-yl]-(4-trifluoromethyl-phenyl)-amine

https://huagongshe.com/de/reaction/60198

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(Trifluoromethyl)anilineHCID 9964—
Eduktp-Toluenesulfonic acid monohydrateHCID 521998—
Edukt7-Chloro-2-(2,6-dichlorobenzyl)oxazolo[5,4-d]pyrimidineHCID 57742456—
LösungsmittelTolueneHCID 1140—
Produkt[2-(2,6-Dichloro-benzyl)-oxazolo[5,4-d]pyrimidin-7-yl]-(4-trifluoromethyl-phenyl)-amineHCID 4264213535%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of 7-chloro-2-(2,6-dichloro-benzyl)-oxazolo[5,4-d]pyrimidine (42 mg, 0.13 mmol), 4-trifluoromethyl-phenylamine (22 mg, 0.13 mmol), and p-TsOH.H2O (51 mg, 0.27 mmol) in toluene (2 mL) was heated to 120° C. in a sealed tube. After 2 h, the solution was cooled purified by preparative reverse-phase HPLC to afford the title compound as a colorless solid (20 mg, 34%). MS (ESI): mass calcd. C19H11Cl2F3N4O, 438.0; m/z found, 439.1 [M+H]+. 1H NMR (CDCl3): 8.57 (s, 1H), 7.90 (d, J=8.6 Hz, 2H), 7.76 (s, 1H), 7.62 (d, J=8.6 Hz, 2H), 7.42 (d, J=8.0 Hz, 2H), 7.31-7.27 (m, 1H), 4.66 (s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440978B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-91b3e372035c44e0b6e444ae7ba999c1
Quellennotizuspto-grants-2016_09