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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388942Generated: October 30, 2026

2-Isopropylaniline → HCID 178438961, compound

https://huagongshe.com/reaction/388942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IsopropylanilineHCID 12561—
Reactant2-ChlorobenzimidazoleHCID 78572—
ReactantHCID 178526482HCID 178526482—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178438961HCID 178438961—

Reaction Steps

To a solution of 2-chloro-5-nitro-1H-benzimidazole (1.5 mmol; prepared from nitration of 2-chloro-1H-benzimidazole; Galy et al, J. Heterocycl. Chem. 1997, 34, 6, 1781-1788) in dry NMP (3 mL) was added 2-isopropylaniline (4 mmol). The resulting solution was subjected to microwave irradiation at 150° C. for 1 h. The contents were cooled to room temperature, diluted with water (20 mL) and extracted with EtOAc (2×15 mL). The combined extracts were then washed with water (20 mL) and brine (20 mL) and dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue obtained was purified by silica gel chromatography using EtOAc/hexane as eluent to obtain (2-isopropylphenyl)-(5-nitro-1H-benzimidazol-2-yl)-amine as light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377983B2
Source datasetuspto-grants-2013_02
ORD IDord-a350f80c87904875a96789269be28b53
Source noteuspto-grants-2013_02