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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433650Generated: October 28, 2026

Ammonium Chloride → 2-Ethoxy-5-(4-ethyl-1-piperazinylsulfonyl)benzamidine

https://huagongshe.com/reaction/433650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Ethoxy-5-(4-ethyl-1-piperazinylsulfonyl)benzonitrileHCID 9967011—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
Product2-Ethoxy-5-(4-ethyl-1-piperazinylsulfonyl)benzamidineHCID 1013206228.6%

Reaction Steps

Trimethylaluminium (10 mL, 2 Molar solution in hexanes) was added dropwise to a slurry of ammonium chloride (1.07 g, 0.02 Mol) in toluene (15 mL) at 0° C. The mixture was stirred without cooling until gas evolution stopped. 2-ethoxy-5-(4-ethyl-1-piperazinylsulfonyl)benzonitrile (the compound of Preparation 7) (3.23 g, 0.01 Mol) was then added and was washed in with toluene (5 mL) before the reaction was stirred at 80° C. for 40 h. After cooling to room temperature silica gel (15 g) and dichloromethane (100 mL) were added. The mixture was then filtered and the solids were washed with dichloromethane/methanol mixtures. The combined filtrate and washings were evaporated and the residue was chromatographed over silica gel using dichloromethane methanol mixtures to afford 1.08 g, 28.6% of the title compound. M/Z=found 341 (M+H). 1H NMR (CD3OD) 1.28 (t, 3H) 1.49 (t, 3H) 2.97 (q, 2H) 3.14 (br, s, 4H) 3.33 (br, s, 4H) 4.32 (q, 2H) 7.45 (d, 1H) 7.96 (d, 1H) 8.05 (dd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667398B2
Source datasetuspto-grants-2003_12
ORD IDord-4645db8bd05e48a6adfa5ba59d1a3240
Source noteuspto-grants-2003_12