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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29147Erstellt: 23. Oktober 2026

Dimethylformamide → 1-(Methylsulfonyl)-1H-Benzimidazol-2-Amine

https://huagongshe.com/de/reaction/29147

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt2-AminobenzimidazoleHCID 13624—
EduktMethanesulfonyl chlorideHCID 31297—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(Methylsulfonyl)-1H-Benzimidazol-2-AmineHCID 2299704528,7%

Reaktionsschritte

2-amino-benzimidazole (1.0 g, 7.5 mmol) was dissolved in 15 mL of anhydrous CH2Cl2 and 3 mL anhydrous DMF and cooled to ˜0° C. Trethylamine (1.6 mL, 1.5 eq.) was added followed by an addition of methanesulfonylchloride (580 μL, 7.5 mmol) over ˜1 minute. After 1 minute at ˜0° C., the reaction was warmed to RT. After 1 hour the reaction was quenched with water, and partitioned between a saturated sodium bicarbonate solution and CH2Cl2. The aqueous layer was extracted with CH2Cl2 and the combined organic layers were washed with water (2 times), brine then dried over NaSO4, filtered and the solvent was removed in vacuo to give 455 mg of N-methanesulfonyl-2-aminobenzimidazole. HPLC shows the material to be 91% pure, (ret. time=3.70). LCMS: obs. M+H@ 212.1 amu. The material was carried on without purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419967B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-457a04e2ceaa47618209d9626c06d3bb
Quellennotizuspto-grants-2008_09