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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884105Generated: October 31, 2026

Sodium borohydride → Methyl 3-[4-(5-aminopyridin-2-ylsulfanyl)phenyl]propionate

https://huagongshe.com/reaction/884105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 3-[4-(5-nitropyridin-2-ylsulfanyl)phenyl]propionateHCID 68525632—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductMethyl 3-[4-(5-aminopyridin-2-ylsulfanyl)phenyl]propionateHCID 68526023—

Reaction Steps

To a solution of methyl 3-[4-(5-nitropyridin-2-ylsulfanyl)phenyl]propionate (2.97 g, 9.33 mmol) in methanol (50 mL) were added sodium borohydride (0.590 g, 15.6 mmol) and 10% palladium-carbon (1.80 g), and the resulting solution was stirred for 24 hours at room temperature under a hydrogen atmosphere at atmospheric pressure. The reaction solution was filtered through Celite, and to the resulting filtrate was added concentrated hydrochloric acid (1.5 mL), and concentrated under reduced pressure. To the residue was added a saturated sodium bicarbonate solution, and extracted with ethyl acetate, and the ethyl acetate layer was washed with brine. The ethyl acetate layer was dried over anhydrous magnesium sulfate, and evaporated, to thereby yield 2.49 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236826B2
Source datasetuspto-grants-2012_08
ORD IDord-799e0954f1aa464c955709c00ba60b78
Source noteuspto-grants-2012_08