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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299161Generated: October 30, 2026

Hydrochloric Acid → 7-Iodo-1H-benzimidazol-5-amine

https://huagongshe.com/reaction/2299161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantStannous chloride dihydrateHCID 61436—
Reactant2-Iodo-4,6-dinitroanilineHCID 18379871—
ReactantEthylacetate methanolHCID 21584119—
Product7-Iodo-1H-benzimidazol-5-amineHCID 1837984833%

Reaction Steps

A solution of 10 g of SnCl2.2H2O and 20 ml of HCl was added into 2,4-dinitro-6-iodoaniline (4.1 g, 13 mmol) and resulting reaction mixture was stirred at reflux for 48 h. The reaction mixture was then basified by adding 15% aq. NaOH and extracted with CHCl3 several times. Combined extracts were dried over MgSO4 and concentrated in vacuo, yielding. oily residue which was subjected to column chromatography (5% MeOH/EtOAc) to yield 1.1 g (4.4 mmol, 33%) of the amine. The amine was stirred at ref lux in 10 ml of formic acid and 10 ml of acetic anhydride for 12 h. The reaction mixture was concentrated in vacuo to yield an oily residue which was stirred in 30 ml of HCl sat'd EtOH for 2 h. The oily reaction mixture after concentration was subjected to column chromatography (5% NH3 sat'd MeOH/EtOAc) to provide 0.69 g (2.7 mmol, 60%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495583B1
Source datasetuspto-grants-2002_12
ORD IDord-ec272c038c8f48bb8c7b101fca396e99
Source noteuspto-grants-2002_12