戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 841537作成日:2026年10月26日

Sodium hydride → 1-(2,6-Difluorobenzyl)-2-(2-Fluoro-6-Methoxylphenyl)-4-Nitrobenzimidazole

https://huagongshe.com/reaction/841537

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物1-(2,6-Difluorobenzyl)-2-(2,6-difluorophenyl)-4-nitrobenzimidazoleHCID 492670—
反応物2-(Bromomethyl)-1,3-difluorobenzeneHCID 581435—
反応物Ethyl acetate hexaneHCID 21226206—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2,6-Difluorobenzyl)-2-(2-Fluoro-6-Methoxylphenyl)-4-NitrobenzimidazoleHCID 22482453—

反応手順

To 1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-4-nitrobenzimidazole (2.00 g, 8 mmol)was added 2,6-difluorobenzylbromide (2.0.2 g, 9.76 mmol, 130 M%) dissolved in THF (20 mL) was added NaH (0.84 g, 21 mmol, 290 M%). After 8 h, the reaction was quenched with m ethanol and concentrated. The residue was dissolved in CH2Cl2, and washed with water and NaCl (sat. aq.). The combined washings were dried (Na2SO4), filtered, concentrated. The crude product was purified by flash chromatography eluting with ethylacetate:hexane (1:1) (2.33 g, 5.64 mmol, 78%). M.p. 189-192° C. 1H-NMR (200 MHz, CD2Cl2) δ8.11 (dd, J=8.1, 1.0 Hz, 1H, H5), 7.84 (dd, J=8.1, 1.0 Hz, 1H, H7), 7.52 (m, 1H, H4′), 7.40 (dd, J=8.1 Hz, 1H, H6), 7.26 (m, 1H, H4″), 6.89-6.74 (m, 4H, H3′,5′,35″,5″), 5.36 (d, J=3.4 Hz, 2H, CH2PhF2 (rotamers)), 3.73 (s, 3H, OCH3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06369235B1
出典データセットuspto-grants-2002_04
ORD IDord-fecc842ecb354c87a71827db06611401
出典メモuspto-grants-2002_04