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HRID 1831931作成日:2026年10月27日

Ammonia → 1-(3-Aminomethyl-2-fluorobenzyl)-3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one

https://huagongshe.com/reaction/1831931

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物3-bromo-1-(3-bromomethyl-2-fluorobenzyl)-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-oneHCID 22050486—
溶媒MethanolHCID 887—
生成物1-(3-Aminomethyl-2-fluorobenzyl)-3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-oneHCID 1141962760%

反応条件

温度80 °C

反応手順

A sealed tube containing a solution of 3-bromo-1-(3-bromomethyl-2-fluorobenzyl)-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one (0.24 g, 0.45 mmol) and NH3 (24 mL of a 7 N solution in MeOH, 168 mmol) was heated at 80° C. for 1 h. The reaction mixture was cooled to room temperature and the solvent was removed under reduced pressure. Purification by flash column chromatography (silica, eluent 99.5:0.5 to 96:4 methylene chloride/methanol) afforded a white solid (0.12 g, 60%): mp 160-163° C.; 1H NMR (300 MHz, CDCl3) δ 7.46-7.45 (m, 1H), 7.44-7.35 (m, 2H), 7.34-7.26 (m, 1H), 7.15-7.05 (m, 1H), 6.95-6.80 (m, 2H), 6.11 (d, J=9 Hz, 1H), 5.21 (s, 2H), 5.19 (s, 2H), 3.90 (s, 2H). ES HRMS m/z 453.0442 (M+H C20H17BrF3N2O2 requires 453.0420).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07067540B2
出典データセットuspto-grants-2006_06
ORD IDord-5242c2c904764ad2b5435839c0d3aaa0
出典メモuspto-grants-2006_06