HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015709Generated: October 31, 2026
Ethyl Acetate → 1-[3-Bromo-4-(methylsulfonyl)benzyl]-5-chloro-2-imino-1,2-dihydropyridine-3-carboxamide hydrochloride
https://huagongshe.com/reaction/1015709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Bromo-4-(bromomethyl)-1-(methylsulfonyl)benzene | HCID 17966908 | — |
| Reactant | 2-Amino-5-chloronicotinamide | HCID 66876883 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[3-Bromo-4-(methylsulfonyl)benzyl]-5-chloro-2-imino-1,2-dihydropyridine-3-carboxamide hydrochloride | HCID 66970057 | 49% |
Reaction Steps
A solution of 2-amino-5-chloronicotinamide (300 mg) and 2-bromo-4-(bromomethyl)-1-(methylsulfonyl)benzene (860 mg) in DMF (5 ml) was stirred at 100° C. for 6 hr. The mixture was allowed to cool to room temperature, ethyl acetate was added, and the precipitated crystals were collected by filtration. The obtained crystals were dissolved in 1N sodium hydroxide solution, and the solution was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate:hexane=9:1→ethyl acetate:methanol=9:1). The obtained yellow solid was dissolved in methanol, 4N hydrogen chloride-ethyl acetate solution was added, and the precipitated crystals were collected by filtration, and recrystallized to give the title compound (195 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985862B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-2a362874c1454337855dec21fb437828 |
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| Source note | uspto-grants-2011_07 |
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