HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → N6-Propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine hydrogen chloride (1:2)
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 2-Amino-4,5,6,7-tetrahydro-6-(propylamino)benzothiazole sulfonate | HCID 86623290 | — |
| Lösungsmittel | 4,5,6,7-Tetrahydro-N6-propyl-2,6-benzothiazolediamine | HCID 4885 | — |
| Lösungsmittel | Isopropyl Acetate | HCID 7915 | — |
| Produkt | N6-Propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine hydrogen chloride (1:2) | HCID 13670715 | — |
Reaktionsbedingungen
| Temperatur | 15 °C |
|---|
Reaktionsschritte
In another embodiment, of 2-amino-4,5,6,7-tetrahydro-6-(propylamino)benzothiazole sulfonate or halide salts (8) may be converted to an HCl salt using a concentrated solution of HCl and isopropyl acetate (IPAC). In such embodiments, 2-amino-4,5,6,7-tetrahydro-6-(propylamino)benzothiazole sulfonate or halide salt (8) may be dissolved in IPAC and cooled to about 15° C. HCl (gas) may then be bubbled into the slurry for from about 0.5 hours to 3 hours to produce 2-amino-4,5,6,7-tetrahydro-6-(propylamino)benzothiazole dihydrochloride (10), after which the mixture may be filtered, washed with an inert solvent, such as, for example, IPAC and dried under vacuum at room temperature. A detailed example of this synthesis may be found in Example 13.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08519148B2 |
| Quelldatensatz | uspto-grants-2013_08 |
| ORD ID | ord-f9c5fa16aa1d472eb4c38776087d571c |
| Quellennotiz | uspto-grants-2013_08 |