HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxy-2-(phenylamino)-4-(phenylimino)-2-cyclobuten-1-one → 1-[2-Hydroxy-3-(cis-3,5-dimethyl-4-propyl-1-piperazinyl)-4-oxo-2-cyclobuten-1-ylidene]-cis-3,5-dimethyl-4-propylpiperazinium hydroxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxy-2-(phenylamino)-4-(phenylimino)-2-cyclobuten-1-one | HCID 10978329 | — |
| Reactant | (2R,6S)-2,6-Dimethyl-1-propylpiperazine | HCID 28363798 | — |
| Product | 1-[2-Hydroxy-3-(cis-3,5-dimethyl-4-propyl-1-piperazinyl)-4-oxo-2-cyclobuten-1-ylidene]-cis-3,5-dimethyl-4-propylpiperazinium hydroxide | HCID 86736294 | — |
Reaction Steps
A mixture of 1.5 grams of 2-anilino-3-hydroxy-4-(phenylimino)-2-cyclobuten-1-one and 1.9 grams of cis-2,6-dimethyl-1-propylpiperazine is heated at 216°-218° C. for 15 minutes under an atmosphere of dry nitrogen. The product is then isolated as described in Example 5 to give 1-[2-hydroxy-3-(cis-3,5-dimethyl-4-propyl-1-piperazinyl)-4-oxo-2-cyclobuten-1-ylidene]-cis-3,5-dimethyl-4-propylpiperazinium hydroxide inner salt as a pale pinkish brown microcrystalline solid melting at about 202°-204° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04138566 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-d55e7381bd9141ef9f5b61ad6953d41e |
| Source note | uspto-grants-1979_02 |