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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208758Generated: November 2, 2026

Formaldehyde → HCID 66576239, compound

https://huagongshe.com/reaction/2208758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 66576237HCID 66576237—
SolventMethanolHCID 887—
ProductHCID 66576239HCID 6657623950%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-((2-Aminoethyl)(methyl)amino)-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide (0.075 g, 0.199 mmol) was dissolved in methanol (5 mL) and cooled to 0° C., formaldehyde (0.056 g, 1.86 mmol) was added. The resulting reaction mixture was stirred at the same temperature for 30 minutes then sodium cyanoborohydride (0.023 g, 0.366 mmol) was added to above reaction mixture and stirred at room temperature for 4 h. After completion, solvent was removed under reduced pressure and water added before extraction with DCM. The combined organic layers were dried, concentrated and purified by column chromatography to provide 5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-3-((2-(dimethylamino)ethyl)(methyl)amino)-2-methylbenzamide (0.040 g, 50%). LCMS: 405.25 (M+1)+; HPLC: 89.93% (@ 254 nm) (Rt; 4.634); 1H NMR (DMSO-d6, 400 MHz) δ 11.47 (s, 1H), 8.21 (s, 1H), 7.08 (s, 1H), 5.85 (s, 1H), 4.24 (bs, 2H), 2.91 (t, 2H), 2.63 (s, 3H), 2.33-2.35 (m, 2H), 2.11-2.18 (m, 15H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376422B2
Source datasetuspto-grants-2016_06
ORD IDord-f6b1a5716c8449ab9b6eed3cbef0652e
Source noteuspto-grants-2016_06