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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Ethoxy-5-(4-ethyl-1-piperazinylsulfonyl)benzonitrile | HCID 9967011 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Ethoxy-5-(4-ethyl-1-piperazinylsulfonyl)benzamidine | HCID 10132062 | 28.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06667398B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-4645db8bd05e48a6adfa5ba59d1a3240 |
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| Source note | uspto-grants-2003_12 |
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