HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Cyclobutene-1,2-dione, 3,4-dimethoxy- → HCID 18347088, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Cyclobutene-1,2-dione, 3,4-dimethoxy- | HCID 123227 | — |
| Reactant | HCID 18347056 | HCID 18347056 | — |
| Reactant | HCID 18347072 | HCID 18347072 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18347088 | HCID 18347088 | — |
Reaction Steps
In a similar manner to that described in Example (1c), a solution of the mixture (2.15 g) of 3-{(4-methoxyphenyl)-[2-(cyclohexen-1-yl)ethylamino]methyl}phenylamine and 3-[(4-methoxyphenyl)-(2-cyclohexylethylamino)methyl]phenylamine [prepared as described in step (b) above] in methanol (40 ml) and 3,4-dimethoxy-3-cyclobutene-1,2-dione (953 mg) were reacted, to afford a crude product, which was purified by reverse phase medium pressure chromatography using a 50:50 by volume mixture of acetonitrile and an aqueous acetic acid buffer solution (water/acetic acid/triethylamine=1000/2/2) as the eluant, to afford the title compound (815 mg) as a pale orange foamy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-6947f8bb444e49c3ba3b7749173f03d8 |
| Source note | uspto-grants-2001_12 |