Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026422Generated: October 30, 2026

Formaldehyde → (R)-5-Bromo-3-(5-(2,4-dimethylpiperazin-1-yl)pyridin-2-ylamino)-1-methylpyridin-2(1H)-one

https://huagongshe.com/reaction/1026422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantWaterHCID 962—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(R)-5-Bromo-1-methyl-3-(5-(2-methylpiperazin-1-yl)pyridin-2-ylamino)pyridin-2(1H)-oneHCID 86683719—
SolventAcetic acid methanolHCID 10129899—
Product(R)-5-Bromo-3-(5-(2,4-dimethylpiperazin-1-yl)pyridin-2-ylamino)-1-methylpyridin-2(1H)-oneHCID 8668372092.7%

Reaction Steps

A mixture of 109d (500 mg, 1.3 mmol), and 30% formaldehyde (6.5 mmol) in methanol/HOAc (30 mL/3 mL) was stirred at room temperature for 5 minutes, followed by the addition of NaBH3CN (120 mg, 1.9 mmol). The mixture was stirred at room temperature for 4 h. It was cooled to room temperature and H2O (20 mL) was added. The mixture was extracted with DCM (50 mL) three times. The combined organic layer was concentrated under reduced pressure and the residue was purified by column chromatography eluting with 30:1 DCM/methanol to afford 109e as a yellow solid (473 mg, 83%). MS: [M+H]+ 392.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729072B2
Source datasetuspto-grants-2014_05
ORD IDord-8688fe8000c3419aa429c7fc3c0989b7
Source noteuspto-grants-2014_05