HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786771Generated: October 29, 2026
2,6-Dibromopyridine → 6-Bromo-N-[(4-chlorophenyl)methyl]-2-pyridinamine
https://huagongshe.com/reaction/1786771
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | 4-Chlorobenzylamine | HCID 66036 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 6-Bromo-N-[(4-chlorophenyl)methyl]-2-pyridinamine | HCID 57597938 | 100.8% |
Reaction Steps
A microwave vial was charged with 4-chloro benzylamine (700 mg; 5 mmol; 5 equivalents) and 2,6-dibromo pyridine (238 mg, 1 mmol). The reaction mixture was stirred in the microwave at 150° C. for three times ten minutes (200 W maximum). The reaction mixture was diluted with diethyl ether (50 ml), washed with 10% aqueous citric acid, saturated aqueous sodium bicarbonate and brine. The organic was dried over magnesium sulfate and, after filtration, concentrated in vacuo to afford an oil as the title compound (300 mg, 100% yield). LC/MS: 299 [M+H]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07507826B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-04199f77205040b7ad4361bb76c1739f |
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| Source note | uspto-grants-2009_03 |
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