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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746031Generated: October 26, 2026

Iodine → Methyl 4-amino-3,6-dichloro-5-iodopicolinate

https://huagongshe.com/reaction/1746031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantMetaperiodic acidHCID 65185—
ReactantMethyl 4-amino-3,6-dichloropyridine-2-carboxylateHCID 22677331—
SolventMethanolHCID 887—
ProductMethyl 4-amino-3,6-dichloro-5-iodopicolinateHCID 90403719208.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

Methyl 4-amino-3,6-dichloropicolinate (10.0 g, 45.2 millimoles (mmol)), periodic acid (3.93 g, 17.2 mmol), and iodine (11.44 g, 45.1 mmol) were dissolved in methanol (30 mL) and stirred at reflux at 60° C. for 27 h. The reaction mixture was concentrated, diluted with diethyl ether, and washed twice with saturated aqueous sodium bisulfate. The aqueous layers were extracted once with diethyl ether, and the combined organic layers were dried over anhydrous sodium sulfate. The product was concentrated and purified by flash chromatography (silica gel, 0-50% ethyl acetate/hexanes) to provide the title compound as a pale yellow solid (12.44 g, 79%): mp 130.0-131.5° C.; 1H NMR (400 MHz, CDCl3) δ 5.56 (s, 2H), 3.97 (s, 3H); 13C NMR (101 MHz, CDCl3) δ 163.80, 153.00, 152.75, 145.63, 112.12, 83.91, 53.21; EIMS m/z 346.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149038B2
Source datasetuspto-grants-2015_10
ORD IDord-b4e42de0c4784381b229c4d96909a48d
Source noteuspto-grants-2015_10