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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653927Generated: October 31, 2026

Hydrochloric Acid → 3-Iodo-N-(3-methyl-2-pyridinyl)benzenesulfonamide

https://huagongshe.com/reaction/1653927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Amino-3-methylpyridineHCID 15347—
Reactantm-Iodobenzenesulphonyl chlorideHCID 39766—
SolventMethyl Isobutyl KetoneHCID 7909—
Product3-Iodo-N-(3-methyl-2-pyridinyl)benzenesulfonamideHCID 19423394—

Reaction Steps

32.4 g 3-methyl-2-pyridinamine (32.4 g, 0.3 mol) was dissolved in isobutylmethylketone (200 ml) and 3-iodo-benzenesulfonyl chloride (30.2 g, 0.1 mol) was added with stirring. The solution was kept at 40° C. for 8 h and then added to dilute hydrochloric acid. The precipitate was filtered off and the organic phase was separated and evaporated. The residue was combined with the first solid material and recrystallized from ethanol. The crystals were dissolved in 1M sodium hydroxide (about 200? ml) and extracted with isobutylmethylketone (3×100 ml). The aqueous phase was partially evaporated to remove isobutylmethylketone residues. Ethanol (100? ml) was added and the solution acidified with acetic acid. The precipitate was filtered off, washed with water and dried. Yield 23 g, 61%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05403930
Source datasetuspto-grants-1995_04
ORD IDord-6d69cc8de2f046a5bfaf932459d53af5
Source noteuspto-grants-1995_04