HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869728Generated: October 29, 2026
Hydrochloric Acid → HCID 178499132, compound
https://huagongshe.com/reaction/869728
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | methyl (2S)-2-{[N-(tert-butoxycarbonyl)-L-alanyl]amino}-3-oxobutanoate | HCID 86674523 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178499132 | HCID 178499132 | — |
Reaction Steps
A solution of methyl (2S)-2-{[N-(tert-butoxycarbonyl)-L-alanyl]amino}-3-oxobutanoate (3.05 g, 10.1 mmol) and 4N hydrochloric acid in 1,4-dioxane (10 mL) was stirred at room temperature. After being stirred for 1 h at same temperature, the reaction mixture was concentrated in vacuo. A solution of the residue in pyridine (50 mL) was heated at 60° C. for 4 h. After being cooled to ambient temperature, the mixture was concentrated in vacuo. The residue was poured into water, and the mixture was extracted with dichloromethane. The organic layer was washed with saturated brine, dried over magnesium sulfate, filtrated and concentrated in vacuo. The residue was triturated with hexane-ethyl acetate (1:1) to give methyl 6-hydroxy-3,5-dimethylpyrazine-2-carboxylate. MS (APCI): m/z 183 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969376B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-08c8b399f72e42feab2cd18ef302586f |
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| Source note | uspto-grants-2015_03 |
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