Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 11630008 | HCID 11630008 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13236344 | HCID 13236344 | — |
Reaction Steps
A mixture of 1.22 ml of acetic anhydride and 0.5 ml of formic acid was stirred at 50°-60° C. for 2 hours. After cooling to room temperature, 1.0 g of 5-piperazinyl-3,4-dihydrocarbostyril was added portionwise to the reaction mixture, during which operation the product was solidified. To the solids was added 5 ml of dichloromethane and the mixture was stirred at room temperature for 2 hours. Then, a large amount of water was added thereto and the mixture was extracted with chloroform. After washing with water, the extract was dried over anhydrous sodium sulfate followed by removal of chloroform by distillation. Recrystallization of the residue from methanol gave 420 mg of 5-(4-formyl-1-piperazinyl)-3,4-dihydrocarbostyril, m.p. 263°-265° C., colorless granules.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04415572 |
|---|
| Source dataset | uspto-grants-1983_11 |
|---|
| ORD ID | ord-e1133232cfc048f2bf2ece0fe62b5343 |
|---|
| Source note | uspto-grants-1983_11 |
|---|