HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 178527432, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 178418806 | HCID 178418806 | — |
| Catalyst | Copper | HCID 23978 | — |
| Product | HCID 178527432 | HCID 178527432 | — |
Reaction Steps
Namely, (1) according to Reaction scheme 4, an aminopyrazole 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 used usually for diazonium decomposition such as a copper salt or the like, to afford a corresponding pyrazolesulfonyl 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 | US04844728 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-1706363585de4458bf652a1b85cc2fec |
| Source note | uspto-grants-1989_07 |