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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 254266Erstellt: 25. Oktober 2026

Ammonium Chloride → 3-[4-Chloro-3-(1-hydroxyethyl)phenyl]-1-(3,3-diphenylpropyl)-1-(2-morpholin-4-ylethyl)urea

https://huagongshe.com/reaction/254266

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt3-(4-Chloro-3-formylphenyl)-1-(3,3-diphenylpropyl)-1-(2-morpholin-4-ylethyl)ureaHCID 16737129—
EduktMagnesium methylbromideHCID 86584079—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-[4-Chloro-3-(1-hydroxyethyl)phenyl]-1-(3,3-diphenylpropyl)-1-(2-morpholin-4-ylethyl)ureaHCID 1673715367%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

16 mg (0.033 mmol, 1 eq.) of 3-(4-chloro-3-formylphenyl)-1-(3,3-diphenylpropyl)-1-(2-morpholin-4-ylethyl)urea (obtained in Example 63) are dissolved in 0.7 mL of dry THF. Once the solution has been cooled to 0° C., 17 μL (0.049 mmol, 1.5 eq.) of magnesium methyl bromide in solution (3 M in diethyl ether) are added to the medium. After stirring for 20 min. at 0° C., the reaction is neutralised with a saturated ammonium chloride solution at 0° C. The aqueous phase is extracted with dichloromethane, the organic phases are washed with brine, dried over MgSO4, filtered and concentrated. The crude reaction product is subjected to chromatography over silica gel (eluent: 1/1 heptane/AcOEt). 11.4 mg of expected product are obtained (yield=67%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07875609B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-aeffb95afd854c909d4eb47d8fd5da6d
Quellennotizuspto-grants-2011_01