HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → HCID 18414393, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 21995390 | HCID 21995390 | — |
| Reactant | HCID 131722572 | HCID 131722572 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 18414393 | HCID 18414393 | — |
Reaction Steps
To a 100 mL three-necked round-bottomed flask equipped with septum and N2 inlet were added 165 mg (0.345 mmol) 2-(2,5-dimethylpyrrol-1-yl)-4-methyl-6-(4-(2-(phenethylpiperazin-4-yl)ethyl)phenyl)-pyridine, 120 mg (1.726 mmol) hydroxylamine hydrochloride, 1 mL water, and 5 mL ethanol. The reaction was refluxed 14 hr, cooled, evaporated, and taken up in ethyl acetate. The organic layer was washed with water and brine, dried over sodium sulfate, and evaporated. The residue was chromatographed on silica gel usirg methanol/methylene chloride as eluant to afford an oil, which was converted to thie hydrochloride salt using 1 N HCl in ether to give 18 mg (10%), mp 242-250° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235747B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-d0f8e1a2b62f4f1ba2880ebdd75644be |
| Source note | uspto-grants-2001_05 |