HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Aminoethyl)-4-(2-methoxyphenyl)piperazine → 3,4,5,7-Tetrahydro-6-carbethoxy-3-[2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl]pyrrolo[3',4':4,5]thieno[2,3-d]pyrimidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Aminoethyl)-4-(2-methoxyphenyl)piperazine | HCID 10399186 | — |
| Reactant | 2-Ethoxymethyleneamino-3,5-dicarbethoxy-4,6-dihydrothieno[3,2-c]pyrrole | HCID 54410789 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3,4,5,7-Tetrahydro-6-carbethoxy-3-[2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl]pyrrolo[3',4':4,5]thieno[2,3-d]pyrimidin-4-one | HCID 15407126 | 48.7% |
Reaction Steps
1.1 g (4.8 mM) of 1-(2-aminoethyl)-4-(2-methoxyphenyl)-piperazine were added to 1.6 g (4.8 mM) of 2-ethoxymethyleneamino-3,5-dicarbethoxy-4,6-dihydrothieno[3,2-c]pyrrole in 25 ml of ethanol and refluxed for 2 h. The mixture was then concentrated in a rotary evaporator, and the crude product was purified by column chromatography (silica gel, mobile phase methylene chloride/methanol 96/4). After recrystallization from ethyl acetate, 1.1 g (47%) of product were isolated with melting point 153-155° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06355647B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-4448ccf54300443883f8be758cfa0479 |
| Source note | uspto-grants-2002_03 |