HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 9H-xanthene-9-carboxylic acid (5-ethyl-[1,3,4]oxadiazol-2-yl)amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 5-Ethyl-1,3,4-oxadiazol-2-amine | HCID 343487 | — |
| Reactant | (3,5-dimethylpyrazol-1-yl)-(9H-xanthen-9-yl)methanone | HCID 4521579 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 9H-xanthene-9-carboxylic acid (5-ethyl-[1,3,4]oxadiazol-2-yl)amide | HCID 53922562 | 41.7% |
Reaction Steps
500.5 mg (1.64 mmol) (3,5-dimethylpyrazol-1-yl)-(9H-xanthen-9-yl)-methanone and 186.8 mg (1.64 mmol) 5-ethyl-[1,3,4]oxadiazol-2-ylamine were suspended in 1.5 ml DMF and stirred for 6 h at 130°. The reaction mixture was allowed to cool to room temperature and 5 ml of acetone were added. After stirring for 5 min, the product was filtered, washed with acetone and dried in vaccuo to yield 219.5 mg of 9H-xanthene-9-carboxylic acid (5-ethyl-[1,3,4]oxadiazol-2-yl)-amide as a white solid, m.p. 256-257° C. and MS: m/e=321.2 (M+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06596743B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-a9df437369a9466ca84aac46592615fe |
| Source note | uspto-grants-2003_07 |