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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1626030Erstellt: 27. Oktober 2026

Pyridine → {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}hexadecanoate

https://huagongshe.com/reaction/1626030

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktDichloromethaneHCID 6344—
EduktPalmitoyl chlorideHCID 8206—
EduktTolvaptanHCID 216237—
LösungsmittelWaterHCID 962—
Produkt{7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}hexadecanoateHCID 8665215174,4%

Reaktionsschritte

Palmitoyl chloride (1.24 ml, 4.4 mmol) was added to a dichloromethane (20 ml) solution of tolvaptan (2.00 g, 4.4 mmol) and pyridine (0.40 ml, 5.0 mmol), and the mixture was stirred at room temperature over night. Water was added to the reaction mixture and the mixture was extracted with dichloromethane. The combined organic layer was washed with water and an aqueous saturated sodium chloride solution, and dried over magnesium sulfate. After filtration and concentration, the residue was purified by silica gel chromatography (n-hexane:ethyl acetate) to thereby obtain 2.25 g (74%) of {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl} hexadecanoate as amorphous.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08785386B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-c42dfcfd72774ff4b76c371b67afaf58
Quellennotizuspto-grants-2014_07