HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494124Generated: October 29, 2026
Hydrazine, acetate (1:1) → HCID 68863971, compound
https://huagongshe.com/reaction/494124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine, acetate (1:1) | HCID 165591 | — |
| Reactant | HCID 58009747 | HCID 58009747 | — |
| Reactant | HCID 68865401 | HCID 68865401 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 68863971 | HCID 68863971 | — |
Reaction Steps
A solution of ethyl 2-methyl-8-(methoxy)-6-[methoxy(oxo)acetyl]-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-7-carboxylate (1.28 g, 3.78 mmol; prepared in a manner similar to that described in Example 62, step 5 to 8, starting with 1-methylpiperazin-2-one (Example 7, step 1 to 3) and hydrazine acetate (1.05 g, 11.36 mmol) in glacial acetic acid (8 mL) was heated at 160° C. in an microwave oven for 20 minutes. The mixture was concentrated under vacuum. The residue was partitioned between chloroform and brine. The organic extract was dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The residue was triturated in a 4:1 mixture of ethanol and diethyl ether. The precipitate was filtered to afford the title compound. ES MS M+1=321
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538112B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-91fb736e81e641519cdf14ef56ffe676 |
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| Source note | uspto-grants-2009_05 |
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