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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323172Generated: October 30, 2026

HCID 2574890, compound → HCID 22010586, compound

https://huagongshe.com/reaction/323172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 2574890HCID 2574890—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 22010728HCID 22010728—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 22010586HCID 2201058658.7%

Reaction Steps

To a mixture of 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(formylmethoxy)phenyl]benzamide (400 mg) and 4-methyl-1-(N-methylamino)methylcarbonylpiperazine (143 mg) in a mixture of methanol (15 ml) and acetic acid (0.5 ml) was added sodium cyanoborohydride (52.4 mg) and the mixture was stirred at ambient temperature for 4 hours. The solution was diluted with ethyl acetate (30 ml) and washed successively with saturated aqueous sodium hydrogen carbonate, water and brine. The organic solution was dried over magnesium sulfate and the solvent was evaporated in vacuo. The residue was purified by silica gel column (chloroform:methanol:conc. ammonia=10:1:0.1) to give 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-[2-[N-methyl-N-(4-methylpiperazin-1-yl)carbonylmethylamino]ethoxy]phenyl]benzamide (310 mg) as a colorless amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211242B1
Source datasetuspto-grants-2001_04
ORD IDord-0d9bdcec637548ee873068e0cbfeb5d3
Source noteuspto-grants-2001_04