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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710746Generated: November 3, 2026

Methyl 4-hydrazinylbenzoate → Methyl 4-(1-(2-(6-methylpyridin-3-yl)ethyl)hydrazinyl)benzoate

https://huagongshe.com/reaction/710746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-hydrazinylbenzoateHCID 408928—
Reactant5-(2-Bromoethyl)-2-methylpyridineHCID 53305856—
SolventTriethylamineHCID 8471—
ProductMethyl 4-(1-(2-(6-methylpyridin-3-yl)ethyl)hydrazinyl)benzoateHCID 6873526828.5%

Reaction Steps

Methyl 4-hydrazinylbenzoate (1 g, 0.005 moles) and 5-(2-bromoethyl)-2-methylpyridine (1 g, 0.005 moles) was taken up in 2.1 mL of triethylamine and stirred at RT for 1 hr. The reaction was then heated at 100 degrees C., overnight. LCMS analysis of the reaction mixtures shows the formation of product. Reaction mixture was concentrated, water (20 mL) was added to the reaction mixture and the mixture extracted with ethyl acetate. The crude product was dissolved in ethyl acetate and purified by column chromatography using neutral alumina, using 100% ethyl acetate as the eluent. After chromatography 400 mg of Methyl 4-(1-(2-(6-methylpyridin-3-yl)ethyl)hydrazinyl)benzoate was obtained, 28.5% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181240B2
Source datasetuspto-grants-2015_11
ORD IDord-611eb678120b445f9ccf77af14b6dea5
Source noteuspto-grants-2015_11