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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2182091Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt1-(2,6-Difluorobenzyl)-2-(2-Fluoro-6-Methoxylphenyl)-4-NitrobenzimidazoleHCID 22482453—
LösungsmittelHydrochloric AcidHCID 313—
Produkt1-(2,6-Difluorobenzyl)-2-(2-Fluoro-4-Methoxylphenyl)-4-AminobenzimidazoleHCID 2248246070%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06894068B2
Quelldatensatzuspto-grants-2005_05
ORD IDord-53052f8c01954de490669692cf69a00a
Quellennotizuspto-grants-2005_05