HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → N-(2-aminoethyl)-4-nitropyridine-2-carboxamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | t-Butyl [2-(4-nitropyridine-2-carboxamido)ethyl]carbamate | HCID 13800214 | — |
| Product | N-(2-aminoethyl)-4-nitropyridine-2-carboxamide hydrochloride | HCID 13800216 | — |
Reaction Steps
7.0 g of t-butyl [2-(4-nitropyridine-2-carboxamido)ethyl]carbamate were stirred at room temperature with 9 ml of methylene chloride and 9 ml of trifluoroacetic acid. Thereafter, the reaction mixture was concentrated under reduced pressure. The residue was converted with hydrogen chloride in ethanol into the hydrochloride and this was recrystallized from ethanol/ether. There was obtained N-(2-aminoethyl)-4-nitropyridine-2-carboxamide hydrochloride as white crystals, m.p. 193°-194°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04764522 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-15105d9027ba4f81884ec22632f6943d |
| Source note | uspto-grants-1988_08 |