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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8220Generated: October 26, 2026

Methanol → 3-Benzyl-4-bromo-butyric acid(1-pyridin-2-yl-2-quinolin-4-yl-ethylidene)-hydrazide

https://huagongshe.com/reaction/8220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPyridineHCID 1049—
Reactant3-Benzyl-4-bromo-butyryl chlorideHCID 21992929—
Reactant(1-Pyridin-2-yl-2-quinolin-4-yl-ethylidene)-hydrazineHCID 73858327—
SolventDichloromethaneHCID 6344—
SolventAmmonium ChlorideHCID 25517—
Product3-Benzyl-4-bromo-butyric acid(1-pyridin-2-yl-2-quinolin-4-yl-ethylidene)-hydrazideHCID 86592623—

Reaction Steps

A solution of (1-pyridin-2-yl-2-quinolin-4-yl-ethylidene)-hydrazine (2.25 g, 8.40 mmol) in anhydrous dichloromethane (100 mL) and pyridine (1.81 mL, 22.4 mmol) is cooled to −78° C., treated with a solution of 3-benzyl-4-bromo-butyryl chloride (2.1 g, 7.8 mmol) in dichloromethane (10 mL), and stirred for 2 h. The mixture is treated with methanol (3 mL), stirred for 10 min, and diluted with saturated ammonium chloride solution (30 mL). The mixture is diluted with dichloromethane (300 mL), washed with water (2×50 mL) and brine (50 mL), dried with anhydrous sodium sulfate, filtered, and concentrated in vacuo. The residue is precipitated from ether to yield the title compound, 2.3 g (60%), as a pale yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087626B2
Source datasetuspto-grants-2006_08
ORD IDord-31b2586fc45a4951aff7c78af74ea681
Source noteuspto-grants-2006_08