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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 3-[4-(5-nitropyridin-2-ylsulfanyl)phenyl]propionate | HCID 68525632 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-[4-(5-aminopyridin-2-ylsulfanyl)phenyl]propionate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08236826B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-799e0954f1aa464c955709c00ba60b78 |
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| Source note | uspto-grants-2012_08 |
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