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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481584Generated: October 27, 2026

Methanol → (2S)-(-)-1-(4-indolyloxy)-3-(4-(4-quinolinyl)piperazin-1-yl)-2-propanol ethanedioate

https://huagongshe.com/reaction/481584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantOxalic AcidHCID 971—
Reactant4-Piperazin-1-yl-quinolineHCID 1534386—
Reactant(2s)-Glycidyl indol-4-yl etherHCID 10943254—
SolventEthyl AcetateHCID 8857—
Product(2S)-(-)-1-(4-indolyloxy)-3-(4-(4-quinolinyl)piperazin-1-yl)-2-propanol ethanedioateHCID 131719669—

Reaction Steps

The title compound was prepared in similar fashion from (S)-(+)-4-(oxiranylmethoxy)-1H-indole and 1-(4-quinolinyl)piperazine. The resulting free base was dissolved in ethyl acetate, and precipitated with one equivalent of oxalic acid in ethyl acetate in 64% overall yield. mp 150°-151°. FDMS m/e=402 (M+ of free base). α[D]589 =-12.41 (c=0.76, methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789402
Source datasetuspto-grants-1998_08
ORD IDord-18678be0665c48e89e671c6083aaa468
Source noteuspto-grants-1998_08