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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980849Generated: October 29, 2026

Cyanogen Bromide → 2-Amino-5-(4-fluorophenylsulfonyloxy)benzimidazole

https://huagongshe.com/reaction/980849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantLuxabendazoleHCID 72019—
SolventMethanolHCID 887—
Product2-Amino-5-(4-fluorophenylsulfonyloxy)benzimidazoleHCID 20221070—

Reaction Steps

14.1 g of 1,2-diamino-4-(4-fluorophenylsulfonyloxy)benzene (see Example 1) and 5.8 g of cyanogen bromide in 150 ml of methanol are heated to reflux for 6 h, then the mixture is cooled and concentrated. The residue is dissolved in water, and ammonia is added with cooling. The precipitated 2-aminobenzimidazole derivative is filtered off with suction, washed with water, dried and recrystallized from ethyl acetate and diisopropyl ether, with the addition of active charcoal; melting point 192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04639463
Source datasetuspto-grants-1987_01
ORD IDord-a3055375963c48ff9048b61c08f3f684
Source noteuspto-grants-1987_01