HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876042Generated: October 25, 2026
N-Iodosuccinimide → 4-Chloro-5-iodopyridin-2-amine
https://huagongshe.com/reaction/876042
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 2-Amino-4-chloropyridine | HCID 581866 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Chloro-5-iodopyridin-2-amine | HCID 21949121 | 67% |
Reaction Steps
4-Chloropyridin-2-amine (0.142 g, 1.10 mmol) and N-iodosuccinimide (0.273 g, 1.22 mmol) were combined in 1.5 mL of acetic acid. The solution was sonicated briefly and then heated to 80° C. After 1 hour the solution was cooled to room temperature and then concentrated under vacuum. After adjusting the pH to ˜8/9 with aqueous ammonia, a light brown solid was collected by filtration. The solid was purified on a 12 g Combiflash column eluting with a gradient of DCM to 5% methanol/0.25% NH4OH (˜28% in water)/DCM. The fractions containing the product were combined and concentrated under vacuum to give 4-chloro-5-iodopyridin-2-amine (187 mg, 67%) as an off-white solid. 1H NMR (500 MHz, DMSO-d6) δ ppm 8.20 (1 H, s), 6.69 (1 H, s), 6.40 (2 H, s); LCMS-ESI (POS), M/Z, M+1: Found 254.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08980903B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-838c5c1aefc84744bbe129feaa0fc173 |
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| Source note | uspto-grants-2015_03 |
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