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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284456Generated: October 31, 2026

Ethyl (7-acetyl-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-4-yl)acetate → Ethyl {7-[(2E)-3-(dimethylamino)prop-2-enoyl]-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-4-yl}acetate

https://huagongshe.com/reaction/2284456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (7-acetyl-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-4-yl)acetateHCID 86731549—
Solvent1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamineHCID 547712—
ProductEthyl {7-[(2E)-3-(dimethylamino)prop-2-enoyl]-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-4-yl}acetateHCID 86731550—

Reaction Conditions

Temperature110 °C

Reaction Steps

The intermediate ethyl (7-acetyl-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-4-yl)acetate 1 g (3.78 mmol) was dissolved in 5 ml of N,N-dimethylformamide ditert butyl acetal and stirred at 110° C. for 6 hours. The reaction mixture was concentrated and then partitioned between H2O and DCM. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to afford the title compound in quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145418B2
Source datasetuspto-grants-2015_09
ORD IDord-cdce99576d51403e948ad23d991d7e8c
Source noteuspto-grants-2015_09