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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274700Generated: October 30, 2026

Triethylamine → 4-[4-(Isoindolin-1-on-2-yl)butylthio]pyridine

https://huagongshe.com/reaction/274700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-[4-(2-Hydroxymethylbenzoyl)aminobutylthio]pyridineHCID 19079154—
SolventDichloromethaneHCID 6344—
Product4-[4-(Isoindolin-1-on-2-yl)butylthio]pyridineHCID 1907907572.1%

Reaction Steps

To a solution of 1.58 g (5.0 mmol) of 4-[4-(2-hydroxymethylbenzoyl)aminobutylthio]pyridine and 2.09 ml (15.0 mmol) of triethylamine in 50 ml of methylene chloride, 0.77 ml (10.0 mmol) of methanesulfonyl chloride was added with stirring at room temperature, and the mixture was stirred at room temperature for 30 minutes. The mixture was washed with saturated aqueous sodium bicarbonate, water and saturated saline, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by column chromatography (eluent: ethyl acetate) to give 1.075 g of the desired compound (72.1% yield, pale brown crystals), mp. 57°-58° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389658
Source datasetuspto-grants-1995_02
ORD IDord-e1f1d983f5fa40b595fdbc806f32613a
Source noteuspto-grants-1995_02