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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 416351Erstellt: 25. Oktober 2026

Tetrahydrofuran → (S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylurea

https://huagongshe.com/reaction/416351

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktDiisopropylethylamineHCID 81531—
Edukt(S)-2-(5-hydroxy-4-(methylamino)pentyl)isoindoline-1,3-dioneHCID 57947589—
Edukt(2-Chloro-3-fluorophenyl)methanamine hydrochlorideHCID 66622557—
Produkt(S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylureaHCID 5794735947%

Reaktionsschritte

To a solution of 4-nitrophenylchloroformate (460 mg, 2.29 mmol) in THF (20 mL) was added 2-chloro-3-fluorobenzylamine hydrochloride (626 mg, 2.29 mmol) and DIEA (0.76 mL, 4.58 mmol) and the mixture was stirred at RT until TLC showed complete consumption of 2-chloro-3-fluorobenzylamine. The mixture was then added into a solution of (S)-2-(5-hydroxy-4-(methylamino)pentyl)isoindoline-1,3-dione (500 mg, 1.91 mmol) in THF (10 mL). The mixture was stirred overnight, concentrated and purified on RP-HPLC using a mixture of acetonitrile and H2O to give (S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylurea (401 mg, 47%). LRMS (M+H+) m/z 448.3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08088793B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-ce77f78f5ef44b46896807ec97909b01
Quellennotizuspto-grants-2012_01