Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tert-Butylamine | HCID 6385 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Perindopril | HCID 107807 | — |
| Lösungsmittel | 2,2-Dimethoxypropane | HCID 6495 | — |
| Produkt | Perindopril Erbumine | HCID 441313 | — |
Reaktionsschritte
Perindopril (I) prepared exactly as per the method described in our pending PCT Application No. PCT/IN03/00042, dated Feb. 28, 2003 and as per the chemistry summarized in Scheme-II and as mentioned hereinbefore in Section 1 (b) was suspended in 2,2-dimethoxypropane (instead of ethyl acetate) to which was gradually tertiary-butylamine. The mixture was heated to reflux till a clear solution was obtained and filtered hot to remove any suspended particles. Thereafter, the solution was cooled to 20° C. to 30° C., and then further cooled to 0° C. to 15° C., maintained at the same temperature for 30 minutes to 1 hour and finally the crystallized solid was filtered and dried at 40-45° C. under vacuum for 5-6 hours to give crystalline perindopril erbumine (IU), exhibiting IR spectra values and, DSC thermogram summarized hereinbelow
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07456296B2 |
|---|
| Quelldatensatz | uspto-grants-2008_11 |
|---|
| ORD ID | ord-45c68e6b42f54ec8bec624d6832c614b |
|---|
| Quellennotiz | uspto-grants-2008_11 |
|---|