HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395861Generated: October 29, 2026
Pyridine → 5-Chloro-2-nitro-n-(2-pyridyl)benzamide
https://huagongshe.com/reaction/395861
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 5-Chloro-2-nitrobenzoic acid | HCID 17286 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Chloro-2-nitro-n-(2-pyridyl)benzamide | HCID 4619650 | 42% |
Reaction Steps
To a stirring solution of 5-chloro-2-nitrobenzoic acid (15 g, 74 mmol) in dichloromethane (300 mL) was added DMF (a few drops) followed by oxalyl chloride (11.3 g, 89 mmol). After stirring for 2 h, the solvent was removed in vacuo and the residue was redissolved in dichloromethane (300 mL). To this stirring solution was added pyridine (17.5 g, 222 mmol), followed by 2-aminopyridine (7 g, 74 mmol). After 24 h, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. The organic phase was separated and washed twice with 1 M citric acid, once with brine, twice with satd aq NaHCO3, and once with brine. The organic phase was then dried (MgSO4), filtered and concentrated in vacuo to a volume of about 25 mL, then diluted with diethyl ether, and sonicated. The resulting precipitate was filtered and dried in vacuo to give 8.63 g (42%) of an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06605626B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-f7596e38ecfc49d88a9af00ccb68e8ae |
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| Source note | uspto-grants-2003_08 |
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