HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexahydro-1,4-diazepine → N,N'-bis[[5-(3,4,5-Trimethoxyphenyl)-thiophen-2-yl]methyl]homopiperazine Dimaleate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | 2-Hydroxymethyl-5-(3,4,5-trimethoxyphenyl)thiophene | HCID 18408492 | — |
| Reactant | 2-Chloromethyl-5-(3,4,5-trimethoxyphenyl)thiophene | HCID 18408530 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N,N'-bis[[5-(3,4,5-Trimethoxyphenyl)-thiophen-2-yl]methyl]homopiperazine Dimaleate | HCID 86758583 | — |
Reaction Steps
2-Hydroxymethyl-5-(3,4,5-trimethoxyphenyl)thiophene (230 mg) was treated in the same manner in Preparation Example 4 to synthesize 2-chloromethyl-5-(3,4,5-trimethoxyphenyl)thiophene. Since this product was unstable, it was immediately reacted with homopiperazine (41 mg) in the same manner in Example 1 without isolating it to obtain a product as a free base. This product was dissolved in methanol, and fumaric acid was added to the solution, thereby converting it into the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06472386B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-e4ca4b5ccfb248a393a17706a874de75 |
| Source note | uspto-grants-2002_10 |