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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17140Generated: October 25, 2026

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

https://huagongshe.com/reaction/17140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant3-(4-Phenoxyphenyl)thieno[3,2-c]pyridin-4-amineHCID 18450763—
SolventDimethylformamideHCID 6228—
Product7-Iodo-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-4-amineHCID 1845087875%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737160B2
Source datasetuspto-grants-2010_06
ORD IDord-dff3e8914e1642b09fc7349c0c1f1600
Source noteuspto-grants-2010_06