HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2,11-dihydro-2-methyl-3H-s-triazolo[3,4-b][3]benzazepin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,11-dihydro-3H-s-triazolo[3,4-b][3]benzazepin-3-one | HCID 13066760 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,11-dihydro-2-methyl-3H-s-triazolo[3,4-b][3]benzazepin-3-one | HCID 13066761 | — |
Reaction Steps
To a solution of 8 parts of 2,11-dihydro-3H-s-triazolo-[3,4-b][3]benzazepin-3-one in 80 volume parts of dimethylformamide is added 9 volume parts of 5N aqueous sodium hydroxide solution and then 3 volume parts of methyl iodide is added dropwise under stirring. After stirring for 1 hour, the reaction mixture is diluted with water and extracted with ethyl acetate. The ethyl acetate layer is washed with water and the solvent is distilled off. The precipitate is collected by filtration to give 2,11-dihydro-2-methyl-3H-s-triazolo[3,4-b][3]benzazepin-3-one as crystals. Recrystallization from isopropyl ether gives light-brown needles melting at 123° -124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002638 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-d48b59df7efa49cf8c9a8645b6cea471 |
| Source note | uspto-grants-1977_01 |