HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478125Generated: November 4, 2026
Hydrochloric Acid → 5-Methanesulfonyl-pyridine-2-carboxylic acid (2-chloro-4-trifluoromethoxy-phenyl)-amide
https://huagongshe.com/reaction/1478125
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Chloro-4-(trifluoromethoxy)aniline | HCID 2734084 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | Methyl 5-(methylsulfonyl)picolinate | HCID 53429647 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Methanesulfonyl-pyridine-2-carboxylic acid (2-chloro-4-trifluoromethoxy-phenyl)-amide | HCID 86709640 | — |
Reaction Steps
2-Chloro-4-trifluoromethoxy-phenylamine (2.0 g, 9.29 mmol) in toluene (50 mL) was added to trimethylaluminum (2.0 M 4.65 mL) then methyl 5-(methylsulfonyl)picolinate 6 (1.0 g, 4.65 mol) was added and the mixture was heated to 80-90° C. for 2 h. The reaction was cooled down and 1N HCl solution (10 mL) was added to be acidic. Dichloromethane (100 mL) was then added and the organic phase was further washed with water (100 mL) and dried over sodium sulfate. The solvent was removed and the residue was mixed with ether (50 mL) and stirred for 0.5 h. The solid was filtered and dried to give 5-methanesulfonyl-pyridine-2-carboxylic acid (2-chloro-4-trifluoromethoxy-phenyl)-amide 7 as a light yellow solid. Yield: 1.26 g, 65%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403812B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-d726d4d36222488c89e40425944a41e5 |
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| Source note | uspto-grants-2016_08 |
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