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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Amino-3-iodo-5-methylthiopyridine | HCID 15486850 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Benzenesulfonylamino-3-iodo-5-methylthiopyridine | HCID 15486851 | 56% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06673797B1 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-fe8b45c9298f4d10830679b155b9d0fe |
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| Source note | uspto-grants-2004_01 |
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