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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2299145Erstellt: 24. Oktober 2026

2-Nitro-1H-benzimidazole → 2-Isopropyl-1H-benzo[d]imidazol-5-amine

https://huagongshe.com/de/reaction/2299145

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Nitro-1H-benzimidazoleHCID 97234—
Edukt2-Isopropyl-5-nitro-1H-benzo[d]imidazoleHCID 683202—
Edukt4-Nitro-1,2-phenylenediamineHCID 5111791—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
LösungsmittelIsobutyric AcidHCID 6590—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-Isopropyl-1H-benzo[d]imidazol-5-amineHCID 82074992%

Reaktionsschritte

A solution of 4-nitro-1,2-phenylenediamine (0.9 g, 5.9 mmol) in 5 ml of isobutyric acid was stirred at reflux for 12 h. The reaction mixture was concentrated in vacuo to yield a dark brown residue, which was dissolved in 100 ml of EtOAc and washed with aqueous NaHCO3. Organic layer was dried over MgSO4 and concentrated in vacuo, yielding an oil which was characterized as 2-isopropyl-5-nitrobenzimidazole and subjected to a following reaction without further purification. The nitrobenzimidazole and 50 mg of 10% Pd-C were dissolved in 100 ml of MeOH and stirred for 12 h under H2. The reaction mixture was filtered and concentrated in vacuo, yielding 0.95 g (5.4 mmol, 92%) of the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06495583B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-d346906e4559426f87e40df4f4b6f597
Quellennotizuspto-grants-2002_12