Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300790Generated: November 1, 2026

5-Aminobenzimidazole → HCID 15549643, compound

https://huagongshe.com/reaction/2300790

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-AminobenzimidazoleHCID 13623—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-2-methylthiopyrimidineHCID 97113—
SolventDimethylformamideHCID 6228—
ProductHCID 15549643HCID 15549643—
ProductHCID 15549644HCID 15549644—

Reaction Steps

To a stirred solution of 5-aminobenzimidazole (700 mg, 5.26 mmol, 1 eq) in DMF (21 mL) was added NaH (231 mg, 5.78 mmol, 1.1 eq, (60% suspension in oil)). The mixture was allowed to stir until gas evolution ceased. To the DMF solution was added 2-methylthio-4-chloropyrimidine (0.612 mL, 5.26 mmol, 1 eq) dropwise via syringe. The mixture was allowed to stir overnight. The DMF was removed under reduced pressure and the residue was diluted with water and extracted 3× with CH2Cl2. The organic extracts were combined, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The mixture was purified by preparative thin layer chromatography (eluted 2× with 3.5% MeOH/CH2Cl2) to give 149 mg 2-methylthio-4-[6-aminobenzimidazol-1-yl]pyrimidine (faster regioisomer) and 89 mg 2-methylthio-4-[5-aminobenzimidazol-1-yl]pyrimidine (slower regioisomer).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498165B1
Source datasetuspto-grants-2002_12
ORD IDord-9626e77457fa46c8ac965fa3dc965d43
Source noteuspto-grants-2002_12