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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36570Erstellt: 24. Oktober 2026

Sulfuryl chloride → 4-Bromoacetyl-2-geranyloxy-2,3,4,5-tetrahydro-1,4-benzothiazepine

https://huagongshe.com/de/reaction/36570

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuryl chlorideHCID 24648—
EduktGeraniolHCID 637566—
Edukt4-Bromoacetyl-2,3,4,5-tetrahydro-1,4-benzothiazepineHCID 15291657—
KatalysatorZincchlorideHCID 3007855—
Produkt4-Bromoacetyl-2-geranyloxy-2,3,4,5-tetrahydro-1,4-benzothiazepineHCID 1529166024,6%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05416066
Quelldatensatzuspto-grants-1995_05
ORD IDord-4a7cf56ef5fc412889de65a617252d8f
Quellennotizuspto-grants-1995_05