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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464979Generated: October 30, 2026

Oxalic Acid → 3,5-diamino-6-chloro-N-2-(2-hydroxy-3-indol-4-yloxy-propylamino)ethyl-pyrazine-2-carboxamide oxalate

https://huagongshe.com/reaction/464979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalic AcidHCID 971—
ReactantIsopropanolHCID 3776—
Reactant4-(oxiran-2-ylmethoxy)-1H-indoleHCID 605015—
Reactant3,5-Diamino-N-(2-aminoethyl)-6-chloropyrazine-2-carboxamideHCID 15148129—
SolventMethanolHCID 887—
Product3,5-diamino-6-chloro-N-2-(2-hydroxy-3-indol-4-yloxy-propylamino)ethyl-pyrazine-2-carboxamide oxalateHCID 20261570—

Reaction Steps

A mixture of 1,2-epoxy-3-(indol-4-yloxy)propane (0.67 g.), 3,5-diamino-6-chloro-N-(2-aminoethyl)pyrazine-2-carboxamide (1.63 g.) and isopropanol (50 ml.) were refluxed together under nitrogen until thin layer chromatography indicated all of the epoxy compound had reacted (about 3 hours). The solvent was removed by rotary evaporator and the resulting yellow solid was chromatographed on silica gel with a 5:1 mixture of chloroform:methanol to give 1.03 g. of product. This material was dissolved in methanol (110 ml.) with warming and the solution was added to oxalic acid (1 equivalent) in methanol (20 ml.). Upon concentration and cooling of the solution, there was obtained 3,5-diamino-6-chloro-N-2-(2-hydroxy-3-indol-4-yloxy-propylamino)ethyl-pyrazine-2-carboxamide oxalate, m.p. 214°-216° C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04550111
Source datasetuspto-grants-1985_10
ORD IDord-d733532a0017426abd2033e559aea6c5
Source noteuspto-grants-1985_10