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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068027Generated: November 2, 2026

4-Chlorobenzylamine → HCID 178522858, compound

https://huagongshe.com/reaction/1068027

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzylamineHCID 66036—
ReactantHCID 178469521HCID 178469521—
SolventDichloromethaneHCID 6344—
ProductHCID 178522858HCID 178522858—

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of ethyl 4-hydroxy-6-(tetrahydro-2H-pyran-4-ylmethyl)-3-quinolinecarboxylate (0.315 g) from Preparation No. 51 and 4-chlorobenzylamine (0.61 nL) is heated to 180° C. for 1 h. The reaction mixture is cooled to 65° C. and diluted with CH2Cl2. Hexanes are added to initiate precipitation of the product. The resulting solid is collected and dried to yield 0.33 g of N-(4-chlorobenzyl)-4-hydroxy-6-(tetrahydro-2H-pyran-4-ylmethyl)-3-quinolinecarboxamide as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248739B1
Source datasetuspto-grants-2001_06
ORD IDord-8fff3fa153414afb85c0946f1519044f
Source noteuspto-grants-2001_06