Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 6-(4-Bromobutyloxy)indanone | HCID 11550940 | — |
| Edukt | 1-(2,3-Dichlorophenyl)piperazine hydrochloride | HCID 11630372 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | HCID 66866083 | HCID 66866083 | — |
Reaktionsschritte
A mixture of 6-(4-bromobutoxy)-indan-1-one prepared by the process described in step (1) above (100 gm, 0.282 mol, 80% purity) and sodium iodide (42 gm, 0.28 mol) in acetonitrile was refluxed for 30 minutes and then cooled to room temperature. 1-(2,3-dichlorophenyl)-piperazine hydrochloride (68 gm, 0.294 mol) and triethyl amine (77 gm, 0.761 mol) were added to the mixture and the resulting mixture was refluxed for 4-6 hr. After solvent was removed, the residue thus obtained was dissolved in chloroform, washed with water which treatment with chloroform and Hydrochloric acid gave 140 g of 6-[4-[4-(2,3-dichlorophenyl)-1-piperazinyl]butoxy]-indan-1-one hydrochloride. This on chloroform solution was basified with ammonium hydroxide to pH 9.5 and extracted with chloroform twice 2×500 ml. The combined chloroform layer was concentrated using rotavapour under reduced pressure to get a residue which on purification with methanol gave 85 gm of 6-[4-[4-(2,3-dichlorophenyl)-1-piperazinyl]-butoxy]-indan-1-one of the formula 2 which has identical characteristic of product obtained for the Example 1, step-2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07872132B2 |
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| Quelldatensatz | uspto-grants-2011_01 |
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| ORD ID | ord-a1de4719d7404802b28903a7d008e2d9 |
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| Quellennotiz | uspto-grants-2011_01 |
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