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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 85627Erstellt: 23. Oktober 2026

Divinyl sulfone → HCID 86676592, Verbindung

https://huagongshe.com/de/reaction/85627

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDivinyl sulfoneHCID 6496—
EduktTriethylamineHCID 8471—
Eduktmethyl 4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(3-aminopropylamino)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysen-9-yl)benzoateHCID 86676591—
LösungsmittelEthanolHCID 702—
ProduktHCID 86676592HCID 8667659283,4%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

Vinylsulfonylethene (5.90 mg, 0.050 mmol) and triethylamine (6.96 μl, 0.050 mmol) were added to a mixture of methyl 4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(3-aminopropylamino)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysen-9-yl)benzoate (15 mg, 0.025 mmol) in EtOH (1 mL). The reaction mixture was heated to 100° C. for 3 hours. The reaction mixture was concentrated under reduced pressure to provide the desired product as a brown solid (15 mg, 76%). LCMS: m/e 719.46 (M+H)+, 3.68 min (method 10).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846647B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-9651d5b1da8f433cb811e2faa8c72009
Quellennotizuspto-grants-2014_09