HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323172Generated: October 30, 2026
HCID 2574890, compound → HCID 22010586, compound
https://huagongshe.com/reaction/323172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 2574890 | HCID 2574890 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 22010728 | HCID 22010728 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22010586 | HCID 22010586 | 58.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211242B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-0d9bdcec637548ee873068e0cbfeb5d3 |
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| Source note | uspto-grants-2001_04 |
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