Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 21423017 | HCID 21423017 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21423021 | HCID 21423021 | — |
Reaction Steps
To a stirred, refluxing solution of 2.2 grams of 3-(4-ethyl-1-piperazinyl)-4-methoxy-3-cyclobutene-1,2-dione dissolved in 30 ml. of absolute ethanol under an atmosphere of dry nitrogen, is added a solution of 1.0 gram of 1-methylpiperazine in 30 ml. of absolute ethanol. The resulting mixture is refluxed for 4 hours and then stripped of solvent under reduced pressure until the volume is approximately 15 ml. The concentrate is treated with decolorizing charcoal and filtered through a bed of diatomaceous earth. Crystallization is induced in the filtrate and the resulting crystalline precipitate is filtered, washed with absolute ethanol, and dried in a steam cabinet. The resulting product, 3-(4-ethyl-1-piperazinyl)-4-(4-methyl-1-piperazinyl)-3-cyclobutene-1,2-dione, is obtained as white crystals melting at about 166.5°-169° C. This product is represented by the following structural formula. ##STR9##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04036828 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-46d26d79f2ac4712a5493ee5c4e65b7f |
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| Source note | uspto-grants-1977_07 |
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