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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209703Generated: November 4, 2026

2-(Chloromethyl)quinoline → Ethyl 2-[[4-methoxybenzenesulfonyl](2-quinolinylmethyl)amino]acetate

https://huagongshe.com/reaction/2209703

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Chloromethyl)quinolineHCID 20394—
ReactantSodium hydrideHCID 24758—
ReactantHCID 3113410HCID 3113410—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-[[4-methoxybenzenesulfonyl](2-quinolinylmethyl)amino]acetateHCID 10573821—

Reaction Steps

To a suspension of sodium hydride (0.84 g, 35.0 mmol) in dimethylformamide (120.0 mL), is added ethyl 2-[[4-methoxybenzenesulfonyl]amino]acetate (3.19 g, 11.67 mmol) and 2-(chloromethyl)quinoline (2.62 g, 12.26 mmol), and the reaction is stirred for three days at room temperature. Then, additional Nail (0.46 g, 11.67 mmol) is added, and the reaction is heated to 50° C. for 5 hours. The reaction is cooled to 0° C., quenched with water, and extracted well with ether. The combined organic layers are washed with brine, dried (Na2SO4), and the solvent is removed to give ethyl 2-[[4-methoxybenzenesulfonyl](2-quinolinylmethyl)amino]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455258
Source datasetuspto-grants-1995_10
ORD IDord-fff3de083c6642f0b5770b9aa7a2df80
Source noteuspto-grants-1995_10