Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | HCID 178470404 | HCID 178470404 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 19378763 | HCID 19378763 | — |
Reaction Steps
To a suspension of 5.45 g of 6-ethoxycarbonyl-5-hydroxy-3-isobutyl-1,2-dihydropyrazin-2-one 4-oxide in chloroform was added dropwise gradually about equivalent quantity of diethyl ether solution of diazomethane at -15° C. 30 Minutes after the addition, 0.5 ml of acetic acid was added to the reaction mixture, and this mixture was allowed to stand for 30 minutes. Then the whole mixture was washed with water, and the solvent was removed by distillation, to the thus obtained residue was added 30 ml of chloroform and dissolved by heating, then 200 ml of diisopropyl ether was added gradually thereto so as to form crystals. The precipitated crystals were collected by filtration, and said operation were repeated twice to obtain 3.10 g of 6-ethoxycarbonyl-3-isobutyl-5-methoxy-l,2-dihydropyrazin-2-one 4-oxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05459142 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-70187683046f4342979590f5dcce9012 |
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| Source note | uspto-grants-1995_10 |
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