HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178480431, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 70246026 | HCID 70246026 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178480431 | HCID 178480431 | 16.1% |
Reaction Steps
230 mg of N-(4-(4-methylhexahydro-1H-1,4-diazepin-1-yl)phenyl]-N-[(7-cyano-2-naphthyl)methyl]sulfamide was dissolved in 9.2 ml of ethanol, to which were added 0.25 ml of triethylamine and 90 mg of hydroxylamine hydrochloride. The mixture was heated for reflux for 2 hours. The reaction mixture was evaporated, and the resulting residue was purified through silica gel column chromatography using an eluent solvent of concentrated ammonia water/methanol/chloroform (0.1/1/7). The solvent was evaporated, and a small amount of aqueous 1 N hydrochloric acid was to the residue, and then evaporated again in vacuo, to obtain 41 mg of N-[(7-hydroxyamidino-2-naphthyl)methyl]-N-[4-(4-methylhexa-hydro-1H-1,4-diazepin-1-yl)phenyl]sulfamide trichloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06333320B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-a38aa2bd42174ab49816ee1a3b288244 |
| Source note | uspto-grants-2001_12 |