HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 20160728, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 20160720 | HCID 20160720 | — |
| Product | HCID 20160728 | HCID 20160728 | — |
Reaction Steps
The sulfamoyl compound (3.7 g, 0.01 m) is suspended in 3N hydrochloric acid, heated to reflux for 16 hours and concentrated in vacuo to give 8-methoxy-1-phenyl-7-sulfamoyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride. 8-Methoxy-1-phenyl-7-sulfamoyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride (3.7 g, 0.01 m) is dissolved in 48% hydrobromic acid (20 ml), refluxed for 2 hours and concentrated in vacuo to afford 8-hydroxy-1-phenyl-7-sulfamoyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrobromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04707483 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-4a8d5863228248d29fa7569fe6188343 |
| Source note | uspto-grants-1987_11 |