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HRID 44887Erstellt: 23. Oktober 2026

1H-1,2,4-Triazole → (S)-2-(2-(3-(1H-1,2,4-triazol-1-yl)phenyl)-1H-imidazol-1-yl)-6a-ethyl-5-methyl-6a,7,8,9-tetrahydropyrrolo[2,1-h]pteridin-6(5H)-one

https://huagongshe.com/de/reaction/44887

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1H-1,2,4-TriazoleHCID 9257—
EduktCesium carbonateHCID 10796—
Edukt1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
Edukt(S)-2-(2-(3-bromophenyl)-1H-imidazol-1-yl)-6a-ethyl-5-methyl-6a,7,8,9-tetrahydropyrrolo[2,1-h]pteridin-6(5H)-oneHCID 58405315—
KatalysatorCopper iodideHCID 83717—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelDimethylacetamideHCID 31374—
Produkt(S)-2-(2-(3-(1H-1,2,4-triazol-1-yl)phenyl)-1H-imidazol-1-yl)-6a-ethyl-5-methyl-6a,7,8,9-tetrahydropyrrolo[2,1-h]pteridin-6(5H)-oneHCID 5840541123%

Reaktionsschritte

(S)-2-(2-(3-bromophenyl)-1H-imidazol-1-yl)-6a-ethyl-5-methyl-6a,7,8,9-tetrahydropyrrolo[2,1-h]pteridin-6(5H)-one (Example 252, 0.118 mmol, 0.050 g) was added to a solution of 1,2,4-triazole (0.593 mmol, 0.041 g), copper iodide (0.007 mmol, 0.001 g), N1,N2-dimethylcyclohexane-1,2-diamine (0.023 mmol, 0.003 g), and Cs2CO3 (0.593 mmol, 0.193 g) in 1 mL of DMA. The reaction mixture was microwaved at 185° C. for 1 h. The reaction mixture was diluted with 15 mL of DCM, washed with 5 mL of water, dried with Na2SO4, filtered and concentrated. The resulting residue was purified by reverse phase HPLC to give the title compound as a white solid (0.012 g, 23%); 1H NMR (400 MHz, CDCl3) δ: 8.83 (s, 1H), 8.12 (m, 2H), 7.95 (s, 1H), 7.90 (m, 1H), 7.69 (s, 1H), 7.60 (m, 3H), 3.37 (m, 4H), 3.20 (m, 1H), 2.35 (m, 1H), 2.26 (m, 3H), 2.00 (m, 2H), 1.77 (m, 1H), 1.62 (m, 1H), 0.78 (t, J=7.4 Hz, 3H); LCMS: 442.3 m/z (M+H)+; ret. Time: 4.722 min (Analytical Method C).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541418B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-cf0a866db12845c79967db5ebae7acb5
Quellennotizuspto-grants-2013_09