HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930468Generated: October 31, 2026
Ammonium Hydroxide → 5-Chloropyridine-2-carboxamide
https://huagongshe.com/reaction/930468
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Chloro-2-picolinic acid | HCID 2762872 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Chloropyridine-2-carboxamide | HCID 21883158 | 87.4% |
Reaction Steps
A 500-mL round-bottomed flask was charged with 5-chloro-2-pyridinecarboxylic acid (Ark Pharm, 10.00 g, 63.5 mmol) and thionyl chloride (Aldrich, 100 ml, 1371 mmol). A catalytic amount of DMF (0.2 ml) was added and the reaction mixture was heated to 80° C. under Argon atmosphere for 4 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The residue was diluted with DCM (100 ml) and added slowly to a stirred solution of ammonium hydroxide (131 ml, 3364 mmol) at 0° C. After completed addition, the reaction mixture was allowed to stir an additional 10 min. The reaction mixture was concentrated under reduced pressure and the precipitate was filtered off. The solid was washed with water and dried to give the title compound (8.686 g, 55.5 mmol, 87% yield) as an off-white solid. MS m/z=157 [M+H]+. Calculated for C6H5ClN2O: 156
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296734B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-5f5fcd6fe9c746d29b5de2ed47fdfc1f |
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| Source note | uspto-grants-2016_03 |
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