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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 242922Erstellt: 26. Oktober 2026

Diisopropylethylamine → [(1R,2R)-2-Benzyloxy-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)propyl]-(7H-purin-6-yl)amine

https://huagongshe.com/reaction/242922

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt6-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purineHCID 97740—
Edukt(1R,2R)-2-Benzyloxy-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)propylamineHCID 68157829—
Lösungsmittel1-ButanolHCID 263—
Produkt[(1R,2R)-2-Benzyloxy-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)propyl]-(7H-purin-6-yl)amineHCID 6815790996,1%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of (1R,2R)-2-benzyloxy-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)propylamine (100 mg, 0.27 mmol), 6-chloro-9-(tetrahydropyran-2-yl)-9H-purine (65 mg, 0.27 mmol) and DIPEA (240 μL, 1.35 mmol) in n-butanol (1 mL) was heated at 90° C. in a sealed vial for 18 h. After cooling to RT, the volatiles were removed in vacuo and the resulting residue loaded onto an Isolute® SCX-2 cartridge then washed with MeOH followed by 2M NH3/MeOH. The product containing fractions were combined and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-10% 2M NH3/MeOH in DCM) to afford the title compound (128 mg, 96%). LCMS (Method J): RT 3.19 min [M+H]+ 494.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653089B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-0327a4b9ab874b37bde8b7d27313d316
Quellennotizuspto-grants-2014_02