HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 14071847, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | HCID 14071840 | HCID 14071840 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14071847 | HCID 14071847 | 57.2% |
Reaction Steps
A mixture of 2.83 g of 1-ethyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid (10 mmol), 1.72 g of anhydrous piperazine (20 mmol), 1.04 g of trimethoxyborane (10 mmol) and 15 ml of acetonitrile was refluxed with heating for 4.5 hours. The reaction solution was cooled to room temperature, 30 ml of water was added therein, and separated crystals were filtered and dried to obtain 2.00 g of the objective compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05869661 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-3f272e38117549d6ad62778dd9221a1e |
| Source note | uspto-grants-1999_02 |