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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272986Generated: October 30, 2026

Formaldehyde → HCID 71765153, compound

https://huagongshe.com/reaction/2272986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 71765148HCID 71765148—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 71765153HCID 71765153—

Reaction Steps

3-(4-Piperidin-4-yl-phenyl)-2H-pyrrolo[1,2-a]pyrazin-1-one (50.0 mg; 0.17 mmol) is dissolved in acetonitrile (1.5 mL), 35% aqueous formaldehyde solution (67.0 μl; 0.84 mmol) is added and the reaction mixture is stirred for 5 min. Sodium cyanoborohydride (21.2 mg; 0.34 mmol) is added in small portions and the reaction stirred for 2 h. The reaction mixture is diluted with water, treated with saturated NaHCO3 solution and extracted with ethylacetate (three times). The combined organic layers are washed with brine, dried over Na2SO4, filtered and evaporated to dryness. The crude product is purified by preparative HPLC. The combined fractions are concentrated in vacuo, the aqueous residue is made basic with saturated NaHCO3 solution, treated with NaCl (solid) and extracted with ethylacetate (four times). The combined organic layers are washed with brine, dried over Na2SO4, filtered off by suction and evaporated to dryness to afford 3-[4-(1-methyl-piperidin-4-yl)-phenyl]-2H-pyrrolo[1,2-a]pyrazin-1-one as beige solid; HPLC/MS 1.28 min (A), [M+H] 308;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120805B2
Source datasetuspto-grants-2015_09
ORD IDord-e41ef95f58ee4c99b0d61d80b885b8c2
Source noteuspto-grants-2015_09