HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → HCID 13923970, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(2-Chlorophenyl)piperazine dihydrochloride | HCID 3018683 | — |
| Reactant | 4H-1-Benzopyran-4-one, 7-(3-chloropropoxy)- | HCID 10847563 | — |
| Catalyst | Sodium Iodide | HCID 5238 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13923970 | HCID 13923970 | — |
Reaction Steps
A mixture of 7-(3-chloropropoxy)-4H-benzopyran-4-one as prepared above in Preparation I (2.38 g; 10 mmol), 1-(2-chlorophenyl)piperazine dihydrochloride (2.96 g; 11 mmol), sodium bicarbonate (3 g; 35 mmol), sodium iodide (0.1 g; 0.6 mmole) in 50 ml dimethylformamide was mechanically stirred and heated at 85°-90° C. for seven hours. The solvent was then evaporated in vacuo and the residue partitioned between water and dichloromethane. The organic phase was treated with an excess of 10% HCl solution in methanol, evaporated in vacuo and the residue recrystallized from ethanol/ethyl acetate to yield 3.2 g of 7-[3-(4-(2-chlorophenyl)-1-piperazinyl)propoxy]-4H-1-benzopyran-4-one as its hydrochloride salt, mp 201°-203° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04678787 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-072b1642352f4ae883db0927ae700dfd |
| Source note | uspto-grants-1987_07 |