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HRID 17140Erstellt: 24. Oktober 2026

N-Iodosuccinimide → 7-Iodo-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-4-amine

https://huagongshe.com/de/reaction/17140

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-IodosuccinimideHCID 120273—
Edukt3-(4-Phenoxyphenyl)thieno[3,2-c]pyridin-4-amineHCID 18450763—
LösungsmittelDimethylformamideHCID 6228—
Produkt7-Iodo-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-4-amineHCID 1845087875%

Reaktionsschritte

A solution of Example 219B (5 g, 15.7 mmol) in DMF (100 mL) was treated with N-iodosuccinimide (4.23 g, 18.8 mmol), stirred at ambient temperature for 2 hours, concentrated to half the original volume, and poured into 5% sodium thiosulfate (400 mL). The mixture was filtered and the filter cake was washed with water and dried. The solids were dissolved in dichloromethane (300 mL), treated with silica gel (80 g), and concentrated. The residue was transferred to a silica gel column (600 g) and chromatographed with ethyl acetate/heptane (1:6) to provide 5.2 g (75%) of the desired product. 1H NMR (CD2Cl2, 400 MHz) δ 7.95 (s, 1H), 7.33-7.29 (m, 4H), 7.12 (s, 1H), 7.10 (t, 1H), 7.02-6.99 (m, 4H), 4.76 (br s, 1H); 13C NMR (CD2Cl2, 400 MHz) δ 158.4, 156.8, 154.7, 154.4, 148.6, 138.4, 131.3, 131.2, 130.4, 124.4, 122.9, 120.0, 119,9, 118.8, 72.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737160B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-dff3e8914e1642b09fc7349c0c1f1600
Quellennotizuspto-grants-2010_06