HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(Trifluoromethyl)-1,3,4-oxadiazol-2-amine → 9H-Xanthene-9carboxylic acid (5-trifluoromethyl-[1,3,4]oxadiazol-2-yl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(Trifluoromethyl)-1,3,4-oxadiazol-2-amine | HCID 522630 | — |
| Reactant | (3,5-dimethylpyrazol-1-yl)-(9H-xanthen-9-yl)methanone | HCID 4521579 | — |
| Product | 9H-Xanthene-9carboxylic acid (5-trifluoromethyl-[1,3,4]oxadiazol-2-yl)-amide | HCID 53955883 | — |
Reaction Steps
The title compound, white solid, m.p. 220-223° C.(decomp.), and MS: m/e=362.2 (M+H+) was prepared in accordance with the general method of example 48a from (3,5-dimethylpyrazol-1-yl)-(9H-xanthen-9-yl)-methanone and 5-trifluoromethyl-[1,3,4]oxadiazol-2-ylamine [U.S. Pat. No. 2,883,391].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06596743B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-74be9b5933b64962bfb4aad2778fc0d8 |
| Source note | uspto-grants-2003_07 |