HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232225Generated: November 1, 2026
Ethanethiol → 1,2,4-Triazolo(3,4-a)phthalazine, 6-(ethylthio)-3-phenyl-
https://huagongshe.com/reaction/2232225
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-chloro-3-phenyl-[1,2,4]triazolo[3,4-a]phthalazine | HCID 1502563 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,2,4-Triazolo(3,4-a)phthalazine, 6-(ethylthio)-3-phenyl- | HCID 3071234 | — |
Reaction Steps
50% Sodium hydride in mineral oil (1 g) is suspended in anhydrous dimethylformamide (50 ml) and stirred for 10 minutes. Then a solution of ethanethiol (1.5 ml) in anhydrous dimethylformamide (10 ml) is slowly added thereto and the resulting mixture is stirred at room temperature for 30 minutes. Finally 6-chloro-3-phenyl-1,2,4-triazolo[3,4-a]phthalazine (5.9 g) is added and the reaction mixture is heated at 50° C. for five hours. The solvent is evaporated off under vacuum and the obtained residue is washed a few times with water and then is crystallized from isopropanol yielding 4.7 g of the compound of the title. M.p. 190°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04788186 |
|---|
| Source dataset | uspto-grants-1988_11 |
|---|
| ORD ID | ord-029b5507b09c49b4981945f6d1b69230 |
|---|
| Source note | uspto-grants-1988_11 |
|---|