HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(2-Nitro-3-pyridinyl)-4-carbobenzoxypiperazine-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Fluoro-2-nitropyridine | HCID 2762802 | — |
| Reactant | 4-((Benzyloxy)carbonyl)piperazine-2-carboxylic acid hydrochloride | HCID 45072677 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(2-Nitro-3-pyridinyl)-4-carbobenzoxypiperazine-2-carboxylic acid | HCID 23339763 | — |
Reaction Steps
A mixture of 2.8 g. of 2-nitro-3-fluoropyridine, 5.0 g. of 4-carbobenzoxypiperazine-2-carboxylic acid, hydrochloride, 25 ml. of triethylamine, and 90 ml. of dimethyl sulfoxide is heated at 55° with stirring for 11/2 hours, then allowed to stand at room temperature overnight. A similar workup to that described in Example 1 gives 4.5 g. of the title product as a viscous orange glass. Thin layer chromatographic analysis of this material shows one single spot.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04138564 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-fae77564f992415f9e7e35f5b8c6ebb1 |
| Source note | uspto-grants-1979_02 |