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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2182091생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/2182091

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1-(2,6-Difluorobenzyl)-2-(2-Fluoro-6-Methoxylphenyl)-4-NitrobenzimidazoleHCID 22482453—
용매Hydrochloric AcidHCID 313—
생성물1-(2,6-Difluorobenzyl)-2-(2-Fluoro-4-Methoxylphenyl)-4-AminobenzimidazoleHCID 2248246070%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06894068B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-53052f8c01954de490669692cf69a00a
출처 메모uspto-grants-2005_05