HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978664Generated: October 30, 2026
Dimethylformamide → HCID 13827299, compound
https://huagongshe.com/reaction/978664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 13827298 | HCID 13827298 | — |
| Reactant | HCID 131715134 | HCID 131715134 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13827299 | HCID 13827299 | — |
Reaction Steps
Trans-6-(2-(4-Carboxyphenyl)ethenyl]-1(2H)-phthalazinone (46 g), thionyl chloride (315 ml) and DMF (2 ml) were mixed and heated slowly to 42° C. and maintained at 42°-48° C. until the gas evolution subsided. The reaction mixture was diluted with toluene and filtered to give the crude acid chloride (52 g). The crude acid chloride (25 g) was dissolved in THF (1250 ml) and 3-dimethylaminopropylamide (250 ml) was added dropwise. After stirring overnight at room temperature the precipitate was filtered, washed with ether (2 l) and then dried to give the amide (13.5 g). The amide was purified via the hydrochloride salt, mp 287° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04665181 |
|---|
| Source dataset | uspto-grants-1987_05 |
|---|
| ORD ID | ord-bc464b8af3f84ab28928e7c470a820b6 |
|---|
| Source note | uspto-grants-1987_05 |
|---|