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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382542Generated: November 1, 2026

Hydrochloric Acid → (E)-2-(3,3-Dimethyl-1-butenyl)-1-(2-pyridyl)-1H-benzimidazole hydrochloride

https://huagongshe.com/reaction/382542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN1-(pyridin-2-yl)benzene-1,2-diamineHCID 752150—
Reactant(E)-1-(2-pyridyl)-2-styryl-1H-benzimidazoleHCID 9796241—
Reactant(E)-4,4-dimethyl-2-pentenoyl chlorideHCID 22736682—
SolventMethanolHCID 887—
Product(E)-2-(3,3-Dimethyl-1-butenyl)-1-(2-pyridyl)-1H-benzimidazole hydrochlorideHCID 22736720—

Reaction Steps

To a solution of (E)-4,4-dimethyl-2-pentenoic acid (Gream, G. E.; Serelis, A. K. Aust. J. Chem. 1978, 31, 863) (200 mg, 1.6 mmol) in benzene (10 ml) was added thionyl chloride (0.5 ml) and the mixture was heated to reflux for 60 min. Volatiles were removed by evaporation to give crude (E)-4,4-dimethyl-2-pentenoyl chloride. Free base of the titled compound was prepared from N-(2-pyridyl)-o-phenylenediamine (150 mg, 0.81 mmol) and (E)-4,4-dimethyl-2-pentenoyl chloride obtained as above according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method A). The free base was dissolved with a 10% methanol solution of hydrogen chloride (5 ml). Concentration and recrystallization from ethyl acetate yielded the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310079B1
Source datasetuspto-grants-2001_10
ORD IDord-ef2d664d3ee3471ca148cb07e54ca822
Source noteuspto-grants-2001_10