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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 544905Erstellt: 25. Oktober 2026

1-Benzofuran-5-carbonyl chloride → 3-(Benzo[b]furan-5-yl-methyl)-4-bromo-1-(beta-D-glucopyranosyl)-indole

https://huagongshe.com/reaction/544905

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Benzofuran-5-carbonyl chlorideHCID 2776268—
Edukt4-bromo-1-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)indoleHCID 67197865—
Produkt3-(Benzo[b]furan-5-yl-methyl)-4-bromo-1-(beta-D-glucopyranosyl)-indoleHCID 67198928—

Reaktionsschritte

The titled compound was prepared from 4-bromo-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)indole obtained in Example 22-(1) and benzo[b]furan-5-carbonyl chloride in a manner similar to Example 27 as a colorless powder. APCI-Mass m/Z 488/490 (M+H). 1H-NMR (DMSO-d6) δ 3.23 (td, J=9.1, 5.5 Hz, 1H), 3.37-3.47 (m, 3H), 3.61-3.69 (m, 2H), 4.39 (s, 2H), 4.53 (t, J=5.5 Hz, 1H), 5.09 (d, J=5.3 Hz, 1H), 5.15 (d, J=5.0 Hz, 1H), 5.22 (d, J=5.9 Hz, 1H), 5.40 (d, J=9.2 Hz, 1H), 6.87 (d, J=1.4 Hz, 1H), 7.04 (t, J=7.9 Hz, 1H), 7.21 (m, 2H), 7.25 (s, 1H), 7.43 (s, 1H), 7.49 (d, J=8.5 Hz, 1H), 7.60 (d, J=8.2 Hz, 1H), 7.93 (d, J=2.1 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07935674B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-c292e9d0a96c4710982699107b982479
Quellennotizuspto-grants-2011_05