HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-[4-(3,4-Methylenedioxybenzoyl)-1-piperazinyl]carbostyril
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Benzodioxole-5-carbonyl chloride | HCID 2734749 | — |
| Reactant | 6-(1-Piperazinyl)carbostyril hydrobromide | HCID 13236367 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-[4-(3,4-Methylenedioxybenzoyl)-1-piperazinyl]carbostyril | HCID 13236358 | 78.1% |
Reaction Steps
6-(1-Piperazinyl)carbostyril hydrobromide (2.0 g) was suspended in 20 ml of DMF. After adding 2.34 ml of triethylamine, a solution of 1.43 g of 3,4-methylenedioxybenzoyl chloride in 2 ml of DMF was added dropwise to the mixture. After completion of addition, the mixture was stirred at room temperature for 30 minutes and the reaction mixture was poured in a large amount of water. Crystals which formed were collected by filtration and dried. Then, the crystals were purified through silica gel column chromatography and recrystallized from chloroform-methanol to give 1.9 g of 6-[4-(3,4-methylenedioxybenzoyl)-1-piperazinyl]carbostyril, m.p. 266°-267° C. (decomp.), yellow powders.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04415572 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-44530a4ccbf9445195e5871d672fd350 |
| Source note | uspto-grants-1983_11 |