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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1932457Generated: November 4, 2026

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

https://huagongshe.com/reaction/1932457

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 numberUS08188277B2
Source datasetuspto-grants-2012_05
ORD IDord-2035eba9467c43fea1841e68f5f4c9df
Source noteuspto-grants-2012_05