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HRID 230714Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-tert-Butyl-1-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-amine

https://huagongshe.com/de/reaction/230714

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktN-{2-tert-Butyl-1-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-yl}acetamideHCID 57723211—
LösungsmittelEthanolHCID 702—
Produkt2-tert-Butyl-1-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-amineHCID 57723213—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

N-{2-tert-Butyl-1′-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-yl}acetamide (500 mg, 1.37 mmol) was dissolved in 10 mL of 1:1/EtOH:2M HCl. The solution was divided into two sealed tubes (5 mL/tube). Each tube was heated at 120° C. in a Personal Chemistry microwaves instrument for 1 h. The fractions were pooled and the solvent was evaporated. The residue was diluted with 2M NaOH and extracted (3×) with EtOAc. The organic phase washed with saturated aqueous NaCl solution and dried over anhydrous Na2SO4. The solvent was evaporated. Yield: 440 mg (99%). 1H NMR (400 MHz, CHLOROFORM-D) δ 1.40-1.52 (m, 2H), 1.52-1.54 (m, 9H), 1.56-1.66 (m, 4H), 1.68-1.75 (m, 2H), 2.07-2.17 (m, 3H), 4.14 (d, J=7.62 Hz, 2H), 6.65 (dd, J=8.50, 2.25 Hz, 1H), 7.04-7.09 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07566788B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-c09f531add384da5b85f028ff65d7eef
Quellennotizuspto-grants-2009_07