HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-[4-(3,4-Dichlorobenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzoyl chloride, 3,4-dichloro- | HCID 76403 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 11630008 | HCID 11630008 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-[4-(3,4-Dichlorobenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril | HCID 13236335 | 26.4% |
Reaction Steps
5-(1-Piperazinyl)-3,4-dihydrocarbostyril (2.6 g) and 4 ml of DBU were added to 40 ml of DMF. The mixture was stirred at room temperature while slowly adding dropwise 10 ml of DMF solution containing 3.0 g of 3,4-dichlorobenzoyl chloride. After completion of addition, the reaction mixture was stirred for 30 minutes. The reaction mixture was poured into a large amount of water and extracted with chloroform. The extract was washed with sodium hydrogencarbonate solution and subsequently with water and dried over anhydrous sodium sulfate. Chloroform was distilled off and residual crystals were recrystallized from methanol to give 1.2 g of 5-[4-(3,4-dichlorobenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril, m.p. 250°-252° C., colorless powders.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04415572 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-3a42d33307c241dd96e6d6adbc499183 |
| Source note | uspto-grants-1983_11 |