HuagongsheHuagongshe Chemistry Print Report · For research reference only
Semicarbazide hydrochloride → 2-(1H-3-Benzazepin-2-yl)hydrazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Semicarbazide hydrochloride | HCID 11236 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 21484983 | HCID 21484983 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(1H-3-Benzazepin-2-yl)hydrazine-1-carboxamide | HCID 13072418 | — |
Reaction Steps
A solution of 24 parts of 2-amino-1H-3-benzazepine hydrobromide, 33 parts of semicarbazide hydrochloride, and 40 parts of potassium acetate in 500 volume parts of methanol is stirred at room temperature overnight. After dilution with water the reaction mixture is neutralized with an aqueous solution of sodium bicarbonate and, then, extracted with chloroform. The chloroform layer is dried over sodium sulfate. Evaporation of the solvent gives 2-semicarbazido-1H-3-benzazepine as crystals. Recrystallization from methanol gives colorless prisms, melting at 188° - 189° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002638 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-77bffb61c8eb4ac3b1f71a7e86d37c6e |
| Source note | uspto-grants-1977_01 |