HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxy-2-(phenylamino)-4-(phenylimino)-2-cyclobuten-1-one → 1-[2-Hydroxy-3-(cis-2,6-dimethyl-4-propyl-1-piperazinyl)-4-oxo-2-cyclobuten-1-ylidene]-cis-2,6-dimethyl-4-propylpiperazinium hydroxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxy-2-(phenylamino)-4-(phenylimino)-2-cyclobuten-1-one | HCID 10978329 | — |
| Reactant | (3R,5S)-3,5-Dimethyl-1-propylpiperazine | HCID 45099431 | — |
| Product | 1-[2-Hydroxy-3-(cis-2,6-dimethyl-4-propyl-1-piperazinyl)-4-oxo-2-cyclobuten-1-ylidene]-cis-2,6-dimethyl-4-propylpiperazinium hydroxide | HCID 86736296 | — |
Reaction Steps
A mixture of 0.48 grams of 2-anilino-3-hydroxy-4-(phenylimino)-2-cyclobuten-1-one and 0.63 grams of cis-3,5-dimethyl-1-propylpiperazine is heated at 230°-240° C. for 10 minutes. The product is then isolated from the reaction mixture according to the procedure described in Example 5 to give 1-[2-hydroxy-3-(cis-2,6-dimethyl-4-propyl-1-piperazinyl)-4-oxo-2-cyclobuten-1-ylidene]-cis-2,6-dimethyl-4-propylpiperazinium hydroxide inner salt melting at about 218°-227° C. This compound has the following formula ##STR3##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04138566 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-fbbb721d2606411bb457833ad269f628 |
| Source note | uspto-grants-1979_02 |