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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 4-(oxiran-2-ylmethoxy)-1H-indole | HCID 605015 | — |
| Reactant | 3,5-Diamino-N-(2-aminoethyl)-6-chloropyrazine-2-carboxamide | HCID 15148129 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3,5-diamino-6-chloro-N-2-(2-hydroxy-3-indol-4-yloxy-propylamino)ethyl-pyrazine-2-carboxamide oxalate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04550111 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-d733532a0017426abd2033e559aea6c5 |
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| Source note | uspto-grants-1985_10 |
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