HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-1,3,4-oxadiazole → 9H-Xanthene-9-carboxylic acid [1,3,4]oxadiazol-2-ylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-1,3,4-oxadiazole | HCID 239787 | — |
| Reactant | 9H-xanthene-9-carbonyl chloride | HCID 2760892 | — |
| Product | 9H-Xanthene-9-carboxylic acid [1,3,4]oxadiazol-2-ylamide | HCID 86585463 | — |
Reaction Steps
The title compound, white solid, m.p. 239-240° C. and MS: m/e=293 (M+) was prepared in accordance with the general method of example 44a from [1,3,4]oxadiazol-2-ylamine and 9-xanthene-carboxylic acid chloride. The [1,3,4]oxadiazol-2-ylamine, white solid, MS: m/e=85 (M+) used in the above reaction was prepared in accordance with the general method of example 44b from formic acid hydrazide and cyanogen bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06462198B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-2c3625b284ee4fb49276715fc2d426fe |
| Source note | uspto-grants-2002_10 |