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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl (7-acetyl-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-4-yl)acetate | HCID 86731549 | — |
| Solvent | 1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamine | HCID 547712 | — |
| Product | Ethyl {7-[(2E)-3-(dimethylamino)prop-2-enoyl]-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-4-yl}acetate | HCID 86731550 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145418B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-cdce99576d51403e948ad23d991d7e8c |
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| Source note | uspto-grants-2015_09 |
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