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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495652Generated: October 28, 2026

1-Chloro-2-(diethylamine)ethane hydrochloride → HCID 22327404, compound

https://huagongshe.com/reaction/495652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2-(diethylamine)ethane hydrochlorideHCID 13363—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22327357HCID 22327357—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 22327404HCID 2232740435%

Reaction Steps

1-(2,4-Dichlorophenyl)-2-oxo-7-(trifluoromethyl)-2,3-dihydro-1H-benzimidazole-5-carbonitrile (0.1541 g) was dissolved in N,N-dimethylformamide (5 ml), and to the solution was added sodium hydride (21.5 mg). The mixture was stirred at room temperature for 5 minutes. To the mixture were added 2-chlorotriethylamine hydrochloride (92.6 mg) and triethylamine (0.087 ml), and the mixture was stirred at 60-70° C. for 15 hours. After allowing to cool, to the reaction mixture was added saturated aqueous sodium bicarbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The resultant residue was dissolved in 2-methyl-2-propanol (10 ml) and heated at 50° C. To the solution was added powdered potassium hydroxide (0.5810 g), and the mixture was stirred for 1 hour. After allowing to cool, to the reaction mixture was added saturated aqueous sodium bicarbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The resultant residue was purified by HPLC using condition 1 to give the title compound (88.3 mg, 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939887B2
Source datasetuspto-grants-2005_09
ORD IDord-1601e5b7bde64da4ae5a3218bf094d30
Source noteuspto-grants-2005_09