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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909253Generated: October 25, 2026

Succinic anhydride → 4-oxo-4-(1-phenyl-3,4-dihydropyrrolo[1,2-a]pyrazin-2(1H)-yl)butanoic acid

https://huagongshe.com/reaction/909253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinic anhydrideHCID 7922—
ReactantTriethylamineHCID 8471—
Reactant1-phenyl-1H,2H,3H,4H-pyrrolo(1,2-a)pyrazineHCID 2770910—
ReactantEthylacetate methanolHCID 21584119—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product4-oxo-4-(1-phenyl-3,4-dihydropyrrolo[1,2-a]pyrazin-2(1H)-yl)butanoic acidHCID 4277933344%

Reaction Steps

1-Phenyl-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine (A2) (396 mg, 2.0 mmol) and NEt3 (277 μl, 2.0 mmol) were added to a suspension of succinic anhydride (176 mg, 1.76 mmol) in MeCN (28 ml), and stirring was carried out for 16 h at RT. The mixture was then diluted with EA (30 ml) and washed with 2N hydrochloric acid (2×5 ml). The organic phase was dried over MgSO4, filtered and concentrated in vacuo. The resulting residue was taken up in EA (50 ml) and again washed with 2N hydrochloric acid (20 ml) and then with a sat. aq. sodium carbonate solution (2×30 ml). The organic phase was again dried over MgSO4, filtered and concentrated in vacuo. CC (EA/MeOH 3:1) with the residue yielded 230 mg (0.77 mmol, 44%) of 4-oxo-4-(1-phenyl-3,4-dihydropyrrolo[1,2-a]pyrazin-2(1H)-yl)butanoic acid (S3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017772B2
Source datasetuspto-grants-2011_09
ORD IDord-471bfbf9f1d94d26aafab6e253d4ad81
Source noteuspto-grants-2011_09