HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 1H-Imidazole-2-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | 2-Aminoimidazole | HCID 82140 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Copper | HCID 23978 | — |
| Product | 1H-Imidazole-2-sulfonyl chloride | HCID 20041793 | — |
Reaction Steps
More specifically, (1) according to Reaction scheme 8, an aminoimidazole is converted into a diazonium salt by using sodium nitrite or the like in hydrochloric acid, hydrobromic acid or the like and then sulfur dioxide is reacted with the resulting diazonium salt in the presence of a catalyst which is usually used for diazonium decomposition such as a copper salt or the like, to afford a corresponding imidazolesulfonyl chloride. With the resulting compound was reacted an aqueous ammonia to give the desired pyrazolesulfonamide (V).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04830660 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-0eaa867749674788968222836fa0b253 |
| Source note | uspto-grants-1989_05 |