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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504044Generated: November 2, 2026

Dimethylformamide → HCID 86613953, compound

https://huagongshe.com/reaction/504044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-MethylbenzaldehydeHCID 10722—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86613954HCID 86613954—
SolventAcetic AcidHCID 176—
ProductHCID 86613953HCID 8661395350.5%

Reaction Steps

To 5-(8-methoxy-1-piperidin-4-ylmethyl-2-oxo-1,2,3,4-tetrahydroquinolin-5-ylmethyl)thiazolidine-2,4-dione (20 μmol, 1.0 eq.) was added a DMF (200 μl) solution of 2-methylbenzaldehyde (24 μmol, 1.2 eq) and acetic acid (10 μl). Si-sodium cyanoborohydride was added further thereto. The solution was shaken for several minutes, diisopropylethylamine (30 μl) was added, and a reaction was carried out at room temperature overnight. The resin was removed by filtration and washed with dichloromethane. The solvent was distilled off from the filtrate in a nitrogen gas stream, and the residue was purified by HPLC (UV-trigger, column: CAPCELL PAK C18, UG 120 S-5, 20 mm×50 mm, 0.05% trifluoroacetic acid-H2O, 0.05% trifluoroacetic acid-CH3CN). The structure was confirmed by LC-MS, and freeze-drying was conducted, giving 5-{8-methoxy-1-[1-(2-methylbenzyl)piperidin-4-yl]methyl-2-oxo-1,2,3,4-tetrahydroquinolin-5-ylmethyl}thiazolidine-2,4-dione in 50.5% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777038B2
Source datasetuspto-grants-2010_08
ORD IDord-8d7ff5ef21b14993bb4811e524fbb953
Source noteuspto-grants-2010_08