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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158884Generated: November 3, 2026

Benzaldehyde → HCID 68442225, compound

https://huagongshe.com/reaction/1158884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantTriethylamineHCID 8471—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 11845779HCID 11845779—
SolventEthanolHCID 702—
ProductHCID 68442225HCID 68442225—

Reaction Steps

Et3N (6.27 mL), PhCHO (4.92 mL) were added successively to the EtOH (81 mL) solution of 5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine-2-carboxylic acid ethyl ester, hydrochloride (9.47 g) at room temperature and stirred for 3 h under a nitrogen atmosphere. Then NaBH3CN (2.97 g) was added to the reaction mixture and stirred for 19 h. The mixture was filtered through a pad of Celite and diluted with CH2Cl2 and washed with 50% K2CO3 aq. The organic layer was dried (K2CO3) and filtered. The filtrate was concentrated under reduced pressure. The residue was applied to silica gel column chromatography, then the column was eluted with CHCl3-acetone (1/0˜9/1) and CHCl3-MeOH (19/1˜9/1). The titled compound was obtained as pale yellow crystals (4.16 g, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812014B2
Source datasetuspto-grants-2010_10
ORD IDord-53f682635bb74ea98fdf9c66f3650609
Source noteuspto-grants-2010_10