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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247021Generated: October 29, 2026

N-(5-methylpyridin-2-yl)-2-nitrobenzamide → 2-Amino-N-(5-methyl-2-pyridinyl)benzamide

https://huagongshe.com/reaction/1247021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5-methylpyridin-2-yl)-2-nitrobenzamideHCID 840320—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-N-(5-methyl-2-pyridinyl)benzamideHCID 1137916395%

Reaction Steps

To a stirring solution of N-(5-methylpyridin-2-yl)-2-nitrobenzamide (1.5 g, 5.8 mmol) and Ni(OAc)2.4H2O (2.9 g, 11.7 mmol) in THF (20 mL) and methanol (40 mL) at 0° C. was added, in small portions, sodium borohydride (0.88 g, 23.2 mol). After complete addition and an additional 5 min, the solvent was evaporated in vacuo and the residue was partitioned between ethyl acetate (200 mL) and 50% conc NH4OH (200 mL). The organic phase was separated and washed again with 50% conc NH4OH, followed by brine, then dried with MgSO4, filtered and concentrated in vacuo to give 1.25 g (95%) of a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129245B2
Source datasetuspto-grants-2006_10
ORD IDord-eca3caf0b0374eafb7146ed4de86ef4b
Source noteuspto-grants-2006_10