HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-hydrazino-5-phenyl-3H-1,4-benzodiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 2-amino-5-phenyl-3H-1,4-benzodiazepine | HCID 12569587 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-hydrazino-5-phenyl-3H-1,4-benzodiazepine | HCID 12612389 | — |
Reaction Steps
To a mixture of 2.35 parts of 2-amino-5-phenyl-3H-1,4-benzodiazepine, 50 parts by volume of ethanol and 1.2 parts by volume of glacial acetic acid is added 1.5 parts by volume of 100% hydrazine hydrate and the mixture is stirred for 1 hour at room temperature. Treatment of the mixture in a similar manner to Example 2 yields 2-hydrazino-5-phenyl-3H-1,4-benzodiazepine as white crystals. Recrystallization from a mixture of methylene chloride and benzene yields white crystals melting at 116° to 118° C. (effervescence).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04116956 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-44ac2a2a38ee4f3f895c24e463fb5da4 |
| Source note | uspto-grants-1978_09 |