HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178515078, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzylhydrazine dihydrochloride | HCID 146540 | — |
| Reactant | HCID 178418477 | HCID 178418477 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178515078 | HCID 178515078 | — |
Reaction Steps
To a stirred suspension of dimethyl-7-chloro-4-hydroxyquinoline-2,3-dicarboxylate (5.00 g, 16.90 mM) and benzylhydrazine dihydrochloride (46.15 g, 236.50 mM) in ethanol (100 mL) was added triethylamine (75.8 mL, 541.0 mM). The mixture was heated to give a brown solution which was refluxed for 40 hours during which time a precipitate formed. The suspension was cooled to room temperature and filtered to give the benzylhydrazine salt of the title compound as an impure yellow solid. Multiple crystallizations from ethanolic hydrogen chloride and methanol gave the title compound (0.370 g, 6%) as a white powder, mp 347-350° C.; MS(CI): 354 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06214826B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-f8c16bbecf424a2f81a68afe47b94588 |
| Source note | uspto-grants-2001_04 |