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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 429551Erstellt: 25. Oktober 2026

Methyl iodide → 1-methyl-1H-1,3-benzodiazol-5-amine

https://huagongshe.com/reaction/429551

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
Edukt5-NitrobenzimidazoleHCID 7195—
EduktSodium hydrideHCID 24758—
EduktChloroform methanolHCID 21584188—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-methyl-1H-1,3-benzodiazol-5-amineHCID 31549921%
Produkt1-Methyl-1H-benzimidazol-6-amineHCID 1368028311%

Reaktionsschritte

A solution of 5-nitrobenzimidazole (3.0 g, 18.4 mmol) in 100 ml of THF was stirred with NaH (2.7 g, 36.8 mmol) for 0.5 h at 25° C. To the solution was added methyl iodide (2.0 ml, 20.3 mmol) and resulting mixture was stirred for 12 h. The reaction mixture was concentrated in vacuo to provide an oil, which was dissolved in 200 ml of MeOH and stirred with 0.3 g of 10% Pd/C under H2 for 12 h. The reaction mixture was filtered and concentrated in vacuo, yielding a dark oily residue which was subjected to column chromatography (3% MeOH/CHCl3) to provide 0.69 g (3.9 mmol, 21%) of 1-methyl-5-aminobenzimidazole and 0.36 g (2.0 mmol, 11%) of 3-methyl-5-aminobenzimidazole.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06316637B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-27d1e517041d4ae195c0e0a0f32a5ef1
Quellennotizuspto-grants-2001_11