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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504045Generated: November 2, 2026

Diisopropylethylamine → HCID 86613955, compound

https://huagongshe.com/reaction/504045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86613954HCID 86613954—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
ProductHCID 86613955HCID 8661395530%

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 tetrahydropyran-4-one (24 μmol, 1.2 eq.) and acetic acid (10 μl). MP-sodium triacetoxy borohydride was added further. After this solution was shaken for several minutes, DIEA (30 μl) was added and a reaction was carried out at 60° C. overnight. The resin was removed by filtration and washed with methylene chloride. The solvent was distilled off with nitrogen gas, 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-(tetrahydropyran-4-yl)piperidin-4-yl]methyl-2-oxo-1,2,3,4-tetrahydroquinolin-5-ylmethyl}thiazolidine-2,4-dione in 30% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777038B2
Source datasetuspto-grants-2010_08
ORD IDord-1ac2926bc88e4e4b9609a0d196bea454
Source noteuspto-grants-2010_08