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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2094250Generated: November 1, 2026

(S)-1-(5-chloro-1H-benzimidazol-2-yl)ethylamine → HCID 178427145, compound

https://huagongshe.com/reaction/2094250

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-1-(5-chloro-1H-benzimidazol-2-yl)ethylamineHCID 42034613—
Reactant3-methyl-4-(4-N-methyl-[1,4]diazepan-1-yl)-benzoic acid chlorideHCID 87248958—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178427145HCID 178427145—

Reaction Steps

489 mg (1.61 mmol) 3-methyl-4-(4-N-methyl-[1,4]diazepan-1-yl)-benzoic acid chloride are placed together with 400 mg (3.96 mmol) TEA in 10 ml THF at ambient temperature and a solution of 433 mg (1.61 mmol) (1S)-1-(5-chloro-1H-benzimidazol-2-yl)-ethyl amine is added dropwise with stirring. After 16 hours stirring at ambient temperature the mixture is evaporated down i. vac., the residue is combined with water and extracted with ethyl acetate. The combined organic phases are washed with sat. sodium chloride solution, dried over sodium sulphate and evaporated down i. vac. The residue is purified by chromatography on aluminium oxide (eluant: dichloromethane/methanol 100:1). The fractions evaporated down are treated with ethereal hydrochloric acid, after total concentration evaporated twice with ethyl acetate and diethyl ether and dried i. vac. at 70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445525B2
Source datasetuspto-grants-2013_05
ORD IDord-518fd1704510465a8bfec5c0b969edef
Source noteuspto-grants-2013_05