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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964131Generated: October 31, 2026

Sodium borohydride → 4-[3-(3-Hydroxyisoindolin-1-on-2-yl)propylthio)pyridine

https://huagongshe.com/reaction/964131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1H-Isoindole-1,3(2H)-dione, 2-[3-(4-pyridinylthio)propyl]-HCID 19079118—
SolventEthanolHCID 702—
Product4-[3-(3-Hydroxyisoindolin-1-on-2-yl)propylthio)pyridineHCID 5712250554.4%

Reaction Steps

To a solution of 5.97 g (20.0 mmol) of 4-(3-phthalimidopropylthio)pyridine in 300 ml of ethanol, 1.51 9 (40 mmol) of sodium borohydride was added, and the mixture was stirred at room temperature for 5 hours. The solvent was distilled off and saturated saline was added to the residue. The mixture was extracted with chloroform and the extract was dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:10) to give 3.27 g of the desired compound (54.4% yield, colorless crystals), mp. 132°-134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05767121
Source datasetuspto-grants-1998_06
ORD IDord-05c67728c9fe4b36ac2820886abd17f8
Source noteuspto-grants-1998_06