Reaktion #2359089

Reaktionsgleichung

(4-(2-(3-aminopyrrolidin-1-yl)pyrimidin-5-ylamino)-6-(3-chloro-5-fluoro-4-hydroxyphenyl)quinolin-3-yl)(cyclopropyl)methanone

HCl

→

desired product

Ausbeute 198.0%

(4-(2-(3-aminopyrrolidin-1-yl)pyrimidin-5-ylamino)-6-(3-chloro-5-fluoro-4-hydroxyphenyl)quinolin-3-yl)(cyclopropyl)methanone hydrochloride

Ausbeute 198.0%

Lösungsmittel

diethyl ether

methanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe solvent was removed under reduced pressure

Vorschrift

(4-(2-(3-aminopyrrolidin-1-yl)pyrimidin-5-ylamino)-6-(3-chloro-5-fluoro-4-hydroxyphenyl)quinolin-3-yl)(cyclopropyl)methanone (30 mg, 0.06 mmol) was suspended in methanol (1 mL) at 0° C. followed by dropwise addition of HCl in diethyl ether (2 M) until complete dissolution of the solid was observed. The solvent was removed under reduced pressure to afford the desired product (33 mg, 92%) as a yellow-orange solid: 1H NMR (500 MHz, MeOD) δ 9.31 (br s, 1H), 8.45 (s, 2H), 8.23-8.14 (m, 2H), 8.02 (d, J=8.8 Hz, 1H), 7.26-7.20 (m, 2H), 4.11-4.00 (m, 2H), 3.94-3.73 (m, 3H), 2.83 (br s, 1H), 2.58-2.48 (m, 1H), 2.28-2.17 (m, 1H), 1.22-1.14 (m, 4H), 0.92-0.88 (s, OH). ESI MS m/z 519 [C27H24ClFN6O2+H]+; HPLC>99.0% (AUC), tR=5.18 min.

Quelle