HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → Ethyl [5-(5-bromo-1,3,4-thiadiazol-2-yl)-2H-tetrazol-2-yl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Ethyl5-bromo-1,3,4-thiadiazole-2-carboxylate | HCID 52987824 | — |
| Reactant | 5-Bromo-1,3,4-thiadiazole-2-carboxamide | HCID 53388679 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl [5-(5-bromo-1,3,4-thiadiazol-2-yl)-2H-tetrazol-2-yl]acetate | HCID 59321687 | — |
Reaction Steps
5-Bromo-1,3,4-thiadiazole-2-carboxamide To a solution of ethyl 5-bromo-1,3,4-thiadiazole-2-carboxylate in THF (1.1 M) at room temperature was added concentrated NH4OH (2.9 equiv). The mixture was stirred at room temperature overnight and a precipitate appeared in the aqueous layer. Then the volatile solvent was removed in vacuo. The resulting mixture was diluted with water and the precipitate was collected, washed with water and dried under vacuum to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383643B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-1a60d4d36d3c46b6a0cdb654362e0959 |
| Source note | uspto-grants-2013_02 |