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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7436Erstellt: 23. Oktober 2026

t-Butyl 2-[({2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-fluorobenzyl)oxy]-5-pyrimidinyl}carbonyl)amino]acetate → 2-[({2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-fluorobenzyl)oxy]-5-pyrimidinyl}carbonyl)amino]acetic acid

https://huagongshe.com/de/reaction/7436

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktt-Butyl 2-[({2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-fluorobenzyl)oxy]-5-pyrimidinyl}carbonyl)amino]acetateHCID 9912947—
LösungsmittelTrifluoroacetic acid methylene chlorideHCID 21863450—
Produkt2-[({2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-fluorobenzyl)oxy]-5-pyrimidinyl}carbonyl)amino]acetic acidHCID 2199053782,9%

Reaktionsschritte

t-Butyl 2-[({2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-fluorobenzyl)oxy]-5-pyrimidinyl}carbonyl)amino]acetate (210 mg, 0.4 mmol) was dissolved in trifluoroacetic acid-dichloromethane (4:1, 2 mL) and the mixture was stirred at room temperature for 15 min. The reaction mixture was concentrated under reduced pressure and the precipitated crystals were recrystallized from ethyl acetate to give the title compound (140 mg, 70%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087597B1
Quelldatensatzuspto-grants-2006_08
ORD IDord-f6f742a697e84fcea25f99e5bc06f882
Quellennotizuspto-grants-2006_08