HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407228Generated: October 30, 2026
Iodine → Methyl 4-amino-5-fluoro-6-(3-fluoro-4-(trifluoromethyl)phenyl)-3-iodopicolinate
https://huagongshe.com/reaction/407228
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Metaperiodic acid | HCID 65185 | — |
| Reactant | Methyl 4-amino-5-fluoro-6-(3-fluoro-4-(trifluoromethyl)phenyl)picolinate | HCID 71150567 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-amino-5-fluoro-6-(3-fluoro-4-(trifluoromethyl)phenyl)-3-iodopicolinate | HCID 71150644 | 255.7% |
Reaction Steps
Methyl 4-amino-5-fluoro-6-(3-fluoro-4-(trifluoromethyl)phenyl)picolinate (500 mg, 1.51 mmol) was dissolved in CH3OH (0.6 mL) in a round bottom flask. Periodic acid (123 mg, 0.542 mmol) and iodine (306 mg, 1.204 mmol) were added, and the reaction mixture was heated at reflux with a drying tube for 12 h. The reaction mixture was cooled to room temperature and concentrated in vacuo. The crude product was dissolved in Et2O and washed with 10% sodium thiosulfate (Na2S2O3; 2×5 mL). The organic extracts were combined, dried over anhydrous Na2SO4, filtered, and concentrated providing methyl 4-amino-5-fluoro-6-(3-fluoro-4-(trifluoromethyl)phenyl)-3-iodopicolinate (635 mg, 92%): 1H NMR (400 MHz, DMSO-d6) δ 7.93 (dd, J=14.8, 6.8 Hz, 1H), 7.90-7.82 (m, 2H), 6.89 (s, 2H), 3.88 (s, 3H); 19F NMR (376 MHz, DMSO-d6) δ −60.02 (t, J=12.4 Hz), −115.50 (td, J=12.2, 7.6 Hz), −139.91 (s); ESIMS m/z 459.62 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754229B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-c8b056b8d9f942bd985d29951445250a |
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| Source note | uspto-grants-2014_06 |
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