HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 6-(2-p-Fluorobenzenesulphonamido-indan-5-yl)-4,5-dihydro-pyridazin-3(2H)-on
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | 6-(2-amino-indan-5-yl)-4,5-dihydropyridazin-3(2H)-one | HCID 14071499 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-(2-p-Fluorobenzenesulphonamido-indan-5-yl)-4,5-dihydro-pyridazin-3(2H)-on | HCID 14071521 | — |
Reaction Steps
2.9 g (12.6 mmol) of 6-(2-amino-indan-5-yl)-4,5-dihydropyridazin-3(2H)-one are dissolved in a mixture of 30 ml of dioxan and 10 ml of acetone, and 1.42 g (14 mmol) of triethylamine and 2.8 g of p-fluorobenzenesulphonyl chloride are added. After 2 hours, the mixture is evaporated, water is added to the residue, and the reaction product is filtered off with suction and recrystallised from glacial acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04929754 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-8520357f37cb4141afc28de9c1e96ddf |
| Source note | uspto-grants-1990_05 |