HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Bromoacetamide → s-Triazolo(5,1-a)isoquinoline, 2-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Bromoacetamide | HCID 4353 | — |
| Reactant | s-Triazolo(5,1-a)isoquinoline, 5,6-dihydro-2-phenyl- | HCID 134397 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | s-Triazolo(5,1-a)isoquinoline, 2-phenyl- | HCID 169678 | 79% |
Reaction Steps
A mixture of 0.5 g. (0.002 mole) of 2-phenyl-5,6-dihydro-s-triazolo[5,1-a]isoquinoline and 0.28 g. (0.002 mole) of N-bromoacetamide in 10 ml. of carbon tetrachloride is refluxed for 5 hours. The crystalline precipitate which forms is filtered and dissolved in methylene chloride. The resulting solution is washed with sodium bicarbonate, then the solvent is evaporated off and the obtained residue recrystallized from ethyl acetate. Yield 79%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04075341 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-4ec79afd853a4edab48144e8f03942db |
| Source note | uspto-grants-1978_02 |