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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432204Generated: November 1, 2026

Benzenesulfonyl chloride → 2-Benzenesulfonylamino-3-iodo-5-methylthiopyridine

https://huagongshe.com/reaction/1432204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Amino-3-iodo-5-methylthiopyridineHCID 15486850—
SolventPyridineHCID 1049—
Product2-Benzenesulfonylamino-3-iodo-5-methylthiopyridineHCID 1548685156%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 2-amino-3-iodo-5-methylthiopyridine (7.63 g) in pyridine (30 ml), benzenesulfonyl chloride (7.9 ml) was added at 15 to 30° C. under nitrogen atmosphere and the mixture was stirred at 60° C. for 15 hours. The reaction solution was then poured into a saturated aqueous sodium hydrogencarbonate solution, extracted with dichloromethane, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. A solution of the resulting crude bis(benzenesulfonyl) product in a mixture of methanol/dioxane (1:1, 200 ml) was added a 1N aqueous potassium hydroxide solution (64 ml) at 15 to 30° C. and the mixture was stirred at 60° C. for 1 hour. The reaction solution was then poured into a saturated aqueous sodium hydrogencarbonate solution, extracted with dichloromethane, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was separated using silica gel column chromatography (methanol:chloroform=1:50) to obtain 6.4 g (56%) of the desired product as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612070B2
Source datasetuspto-grants-2009_11
ORD IDord-63f56b16ec644211911b803f487f363a
Source noteuspto-grants-2009_11