HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine hydrate (1:1) → 5-(4-Aminophenyl)-3,4-diazabicyclo[4.1.0]hept-4-en-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 54423379 | HCID 54423379 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(4-Aminophenyl)-3,4-diazabicyclo[4.1.0]hept-4-en-2-one | HCID 20264844 | 95% |
Reaction Steps
20 g (97.5 millimoles) of cis-2-(p-aminobenzoyl)-cyclopropanecarboxylic acid, 5.9 g (118 millimoles) of hydrazine hydrate and 100 ml of ethanol are refluxed for 5 hours. After filtering off the product at 10° C. and drying it under reduced pressure at 50° C., 18.6 g (95% of theory) of 2-(p-aminophenyl)-3,4-diaza-bicyclo[4.1.0]-hept-2-en-5-one are obtained as pale yellow crystals, which are identical with the compound from Example 8a.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04271163 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-dbef9dabf2d14617a39615891871e46f |
| Source note | uspto-grants-1981_06 |