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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine, acetate (1:1)HCID 165591—
ReactantHCID 58009747HCID 58009747—
ReactantHCID 68865401HCID 68865401—
SolventAcetic AcidHCID 176—
ProductHCID 68863971HCID 68863971—

Reaction Conditions

Temperature160 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538112B2
Source datasetuspto-grants-2009_05
ORD IDord-91fb736e81e641519cdf14ef56ffe676
Source noteuspto-grants-2009_05