HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255153Generated: October 30, 2026
Dimethylformamide → HCID 178470316, compound
https://huagongshe.com/reaction/2255153
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 178470403 | HCID 178470403 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178470316 | HCID 178470316 | — |
Reaction Steps
There were mixed 1.00 g of 5-amino-6-ethoxycarbonyl-3-isobutyl-1,2-dihydropyrazin-2-one 4-oxide, 1.18 g of potassium hydrogencarbonate (powder), 20 ml of dry dimethylformamide and 932 μl of benzyl bromide. The mixture was stirred for 16 hours at room temperature to effect a reaction. After completion of the reaction, the reaction mixture was poured into 50 ml of ethyl acetate. The resulting mixture was washed with 30 ml of water three times. The aqueous layer was extracted with 30 ml of ethyl acetate twice. The extract was combined with the above ethyl acetate layer. The combined solution was washed with 30 ml of water twice, and dried over magnesium sulfate. The solvent was removed by evaporation. The residue was recrystallized from ethanol to obtain 1.06 g of 2-amino-5-benzyloxy-3-ethoxycarbonyl-6-isobutylpyrazine 1-oxide (Compound B-10) as pale yellow fine needle-like crystals having a melting point of 114.5°-115.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05238938 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-ec9d5954941c4148a20930837f903ea4 |
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| Source note | uspto-grants-1993_08 |
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