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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880447Generated: October 30, 2026

Acetic Acid → HCID 66914859, compound

https://huagongshe.com/reaction/880447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethylamineHCID 6329—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86654667HCID 86654667—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66914859HCID 6691485930%

Reaction Steps

Acetic acid was added to a solution of methylamine (0.45 mL, 5.30 mmol, 40% in water) in tetrahydrofuran (8 mL) to adjust the pH to 6. A solution of (2-formyl-4-phenyl-pyrrol-1-yl)-acetic acid ethyl ester (680 mg, 2.65 mmol) in tetrahydrofuran (4 mL) was added and the reaction mixture stirred at ambient temperature for 45 min. Sodium cyanoborohydride (0.33 g, 5.30 mmol) was added and the reaction mixture heated at 75 C for 18 h. Concentration in vacuo yielded a residue which was partitioned between water and ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to afford the crude product. Purification by column chromatography over silica gel (100-200 mesh) using 30% ethyl acetate in petroleum ether afforded 2-methyl-7-phenyl-1,2-dihydropyrrolo[1,2-a]pyrazin-3-one (180 mg, 30%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993574B2
Source datasetuspto-grants-2015_03
ORD IDord-4400e04b92524f0d97369014d7312826
Source noteuspto-grants-2015_03