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HRID 841538作成日:2026年10月27日

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

https://huagongshe.com/reaction/841538

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) δ7.45 (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US06369235B1
出典データセットuspto-grants-2002_04
ORD IDord-5d97ad8b85ba4525a9fced76626e05c6
出典メモuspto-grants-2002_04