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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230496Generated: November 1, 2026

Triethylamine → Emedastine

https://huagongshe.com/reaction/2230496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-MethylhomopiperazineHCID 228349—
Reactant2-chloro-1-(2-ethoxyethyl)-1H-benzimidazoleHCID 10489356—
ReactantEthyl acetate hexaneHCID 21226206—
SolventDichloromethane methanolHCID 21226129—
ProductEmedastineHCID 3219—

Reaction Conditions

Temperature70 °C

Reaction Steps

Combine 2-chloro-1-(2-ethoxyethyl)-1H-benzimidazole (22.3 g, 99.4 mmoL), 1-methyl[1,4]diazepane (19 mL, 152.8 mmol), and triethylamine (75 mL). Heat to 70° C. After 18 hours, add 1-methyl[1,4]diazepane (10 mL) and continue to heat at reflux. After 96 hours, cool to ambient temperature and partition the reaction mixture between water and ethyl acetate. Separate the layers and extract the organic layer with a saturated aqueous sodium bicarbonate solution and then brine. Dry the organic layer over MgSO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 50% ethyl acetate/hexane and then 10% methanol/dichloromethane to give 1-methyl-4-(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)[1,4]diazepane: Rf=0.52 (silica gel, dichloromethane/methanol/concentrated aqueous ammonia, 90/10/0.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423704B1
Source datasetuspto-grants-2002_07
ORD IDord-cc26ef8573d74e9986ec2427748b2c13
Source noteuspto-grants-2002_07