HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891891Generated: October 31, 2026
N-Iodosuccinimide → 2-Amino-5-fluoro-3-iodopyridine
https://huagongshe.com/reaction/1891891
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Reactant | 2-Amino-5-fluoropyridine | HCID 2737701 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Amino-5-fluoro-3-iodopyridine | HCID 18455974 | 18% |
Reaction Steps
To a mixture of 2-amino-5-fluoropryidine (2.0 g, 17.8 mmol) and dimethyl sulfoxide (50 mL) was added N-iodosuccinimide (4.8 g, 21.4 mmol), which was stirred for 1 hour at room temperature. A suitable amount of acetic add was added to this mixture, which was stirred for 1 hour at the same temperature, and then stirred for another 3 hours at 55° C. This reaction mixture was cooled to room temperature, after which a saturated sodium hydrogencarbonate aqueous solution was added, and the mixture was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue thus obtained was purified by NH silica gel column chromatography (ethyl acetate) to obtain the title compound (751 mg, 18%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507530B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-07e5cd7483ad4e5c98825a4e0c8644d5 |
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| Source note | uspto-grants-2013_08 |
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