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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 3-(4-Phenoxyphenyl)thieno[3,2-c]pyridin-4-amine | HCID 18450763 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Iodo-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-4-amine | HCID 18450878 | 75% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737160B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-dff3e8914e1642b09fc7349c0c1f1600 |
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| Source note | uspto-grants-2010_06 |
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