HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 242925Erstellt: 26. Oktober 2026
Diisopropylethylamine → [(R)-2-Benzyloxy-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)ethyl]-(7H-purin-6-yl)amine
https://huagongshe.com/reaction/242925
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 6-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine | HCID 97740 | — |
| Edukt | (R)-2-Benzyloxy-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)ethylamine | HCID 68157494 | — |
| Lösungsmittel | 1-Butanol | HCID 263 | — |
| Produkt | [(R)-2-Benzyloxy-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)ethyl]-(7H-purin-6-yl)amine | HCID 68157727 | 64,3% |
Reaktionsschritte
A mixture of (R)-2-benzyloxy-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)ethylamine (298 mg, 0.83 mmol), 6-chloro-9-(tetrahydropyran-2-yl)-9H-purine (200 mg, 0.83 mmol) and DIPEA (700 μL, 4.2 mmol) in n-butanol (5 mL) was heated at 90° C. in a sealed vial for 48 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 as a colourless oil (256 mg, 64%). LCMS (Method B): RT 3.26 min [M+H]+ 480.2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08653089B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-5fdbc1da9afb46c4968c794f45b70cce |
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| Quellennotiz | uspto-grants-2014_02 |
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