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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971463Generated: November 2, 2026

2-Aminobenzimidazole → 1H-benzimidazol-2-ylthiourea

https://huagongshe.com/reaction/1971463

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzimidazoleHCID 13624—
Reactant1,1'-ThiocarbonyldiimidazoleHCID 80264—
ReactantAmmonium AcetateHCID 517165—
SolventAcetonitrileHCID 6342—
Product1H-benzimidazol-2-ylthioureaHCID 2771015—

Reaction Conditions

Temperature90 °C

Reaction Steps

0.535 g (3.0 mmol) N,N′-thiocarbonyldiimidazole was dissolved in 5 ml acetonitrile, and to this yellow solution was added drop-wise 0.40 g (3.0 mmol) 2-aminobenzimidazole, suspended in 5 ml acetonitrile, at room temperature. After 30 minutes, a precipitate formed, and the mixture was stirred another 12 hours. After 0.474 g (6.0 mmol) ammonium acetate in substance (German: “in Substanz”) was added to this mixture, the mixture was heated in the microwave (at 100 Watt) 30 minutes long at 90° C. The solvent was removed under vacuum, water was added to the residue and an extraction with dichloromethane (3×30 ml) followed. The combined organic phase was washed once again with water and, after drying over MgSO4, the solvent was removed under vacuum. The product was purified by means of preparative HPLC (Merck: Chromolith RP-18E, 100-25; eluent wasser/acetonitrile/0.1 molar acetic acid). In this single pot procedure, 0.27 g of the N-1H-benzimidazole-2-ylthiourea was directly recovered without isolation of the intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431604B2
Source datasetuspto-grants-2013_04
ORD IDord-ff9b9afc6d664712aa2db1e6a30c60e3
Source noteuspto-grants-2013_04