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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838312Generated: November 3, 2026

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

https://huagongshe.com/reaction/1838312

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 numberUS06673797B1
Source datasetuspto-grants-2004_01
ORD IDord-fe8b45c9298f4d10830679b155b9d0fe
Source noteuspto-grants-2004_01