HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4D-083
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Oxo-6-phenyl-2,3-dihydropyridazine-4-carboxylic acid | HCID 12148934 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4D-083 | HCID 1475328 | — |
Reaction Steps
In an alternate procedure, a mixture of 2,3-dihydro-3-oxo-6-phenyl-4-pyridazinecarboxylic acid (1.92 g), triethylamine (3.0 ml), and thionyl chloride (5.0 ml) in tetrahydrofuran is allowed to stir at 20°-25° C. for 6 hours. The mixture is concentrated on the rotary evaporator and the residue is treated with 50 ml of cold ammonium hydroxide solution. The solid product is collected and recrystallized from acetic acid to give 2,3-dihydro-3-oxo-6-phenyl-4-pyridazinecarboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04404203 |
| Source dataset | uspto-grants-1983_09 |
| ORD ID | ord-091ee31fa94a4af29767edc1a3780f19 |
| Source note | uspto-grants-1983_09 |