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HRID 2182091作成日:2026年10月25日

Acetic Acid → 1-(2,6-Difluorobenzyl)-2-(2-Fluoro-4-Methoxylphenyl)-4-Aminobenzimidazole

https://huagongshe.com/reaction/2182091

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物1-(2,6-Difluorobenzyl)-2-(2-Fluoro-6-Methoxylphenyl)-4-NitrobenzimidazoleHCID 22482453—
溶媒Hydrochloric AcidHCID 313—
生成物1-(2,6-Difluorobenzyl)-2-(2-Fluoro-4-Methoxylphenyl)-4-AminobenzimidazoleHCID 2248246070%

反応手順

To 1-(2,6-difluorobenzyl)-2-(2-fluoro-4-methoxylphenyl)-4-nitrobenzimidazole (Example 50) (2.00 g, 4.98 mmol) dissolved in acetic acid (20 mL) was added SnCl2x2H2O (9.02 g) dissolved in concentrated HCl (8 mL). After stirring for 30 min at room temperature, the mixture was concentrated. The residue was diluted with CH2Cl2 and washed with NaHCO3 (sat. aq.) and NaCl (sat. aq.). The combined washings were dried (Na2SO4), filtered, and evaporated. The crude product was recrystallized from methanol to give 3.26 g of white crystals, (8.78 mmol, 70% yield). M.p. 200-202° C. 1H-NMR (200 MHz, CD2Cl2) δ 7.45 (m, 1H, H4′), 7.22 (m, 1H, H4″), 7.05 (dd, J=7.8, 7.6 Hz, 1H, H6), 6.85-6.72 (m, 5H, H3″,5″), 6.50 (dd, J=7.7, 1.0 Hz, 1H, H5), 5.21 (d, J=5.4 Hz, 2H, CH2PhF2 (rotamers)), 4.34 (br, 2H, NH2), 3.72 (s, 3H, OCH3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06894068B2
出典データセットuspto-grants-2005_05
ORD IDord-53052f8c01954de490669692cf69a00a
出典メモuspto-grants-2005_05