HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985462Generated: October 29, 2026
Pyridine → N-(3-amino-2-methoxy-5-trifluoromethyl-phenyl)-methanesulfonamide
https://huagongshe.com/reaction/985462
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Methoxy-5-(trifluoromethyl)benzene-1,3-diamine | HCID 22506994 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-amino-2-methoxy-5-trifluoromethyl-phenyl)-methanesulfonamide | HCID 22506980 | 58.2% |
Reaction Steps
2-Methoxy-5-trifluoromethylbenzene-1,3-diamine (2.32 g, 11.3 mmol) was dissolved in 50 mL anhydrous dichloromethane. The solution was cooled to 0° C., and pyridine (3.64 mL, 45.0 mmol) and methane sulfonyl chloride (0.89 mL, 11.5 mmol) were added. The reaction was left to stir overnight at room temperature. A few more drops (˜0.1 mL) of methane sulfonyl chloride were added and the reaction stirred an extra day. Then 200 mL EtOAc, was added and the solution washed once with 100 mL water, twice with 15 mL saturated aqueous NH4Cl solution and finally with brine. The organic solution was dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel using EtOAc/hexanes eluent mixtures, providing N-(3-amino-2-methoxy-5-trifluoromethyl-phenyl)-methanesulfonamide (1870 mg, 6.58 mmol, 58% yield) as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06872726B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-c9af3732abda490ea07deb8d079eaa83 |
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| Source note | uspto-grants-2005_03 |
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