HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sulfuryl chloride → 4-Bromoacetyl-2-geranyloxy-2,3,4,5-tetrahydro-1,4-benzothiazepine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sulfuryl chloride | HCID 24648 | — |
| Edukt | Geraniol | HCID 637566 | — |
| Edukt | 4-Bromoacetyl-2,3,4,5-tetrahydro-1,4-benzothiazepine | HCID 15291657 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Produkt | 4-Bromoacetyl-2-geranyloxy-2,3,4,5-tetrahydro-1,4-benzothiazepine | HCID 15291660 | 24,6% |
Reaktionsschritte
The above-mentioned 4-bromoacetyl-2,3,4,5-tetrahydro-1,4-benzothiazepine (2.5 g) and sulfuryl chloride (1.5 g) were reacted in the same manner as in Experimental Example 7 to give 4-bromoacetyl-2-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepmne (1.4 g). This compound (0.30 g), geraniol (0.30 g) and zinc chloride (0.26 g) were reacted in the same manner as in Experimental Example 9 to give 4-bromoacetyl-2-geranyloxy-2,3,4,5-tetrahydro-1,4-benzothiazepine (0.21 g). Then, this compound (0.21 g), 4-benzyl piperidine (O.11 g) and potassium carbonate (0.13 g) were reacted in the same manner as in Experimental Example 6 to give 4-[1-(4-benzyl) piperidinyl]acetyl-2-geranyloxy-2,3,4,5-tetrahydro-1,4-benzothiazepine (0.26 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05416066 |
| Quelldatensatz | uspto-grants-1995_05 |
| ORD ID | ord-4a7cf56ef5fc412889de65a617252d8f |
| Quellennotiz | uspto-grants-1995_05 |