HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363050Generated: October 29, 2026
Methanamine, N-methoxy-, hydrochloride (1:1) → 3-(4-Chloro-3-trifluoromethyl-benzenesulfonylamino)-5-methyl-pyridine-2-carboxylic acid methoxy-methyl-amide
https://huagongshe.com/reaction/1363050
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | HCID 57870807 | HCID 57870807 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Chloro-3-trifluoromethyl-benzenesulfonylamino)-5-methyl-pyridine-2-carboxylic acid methoxy-methyl-amide | HCID 57870808 | 84.1% |
Reaction Steps
10.49 g (26.6 mmol) of 3-(4-chloro-3-trifluoromethyl-benzenesulfonylamino)-5-methyl-pyridine-2-carboxylic acid was reacted with 5.40 g (33.2 mmol) of N,N′-carbonyldiimidazole in 40 mL of refluxing THF for 3 h. The temperature was lowered to 50° C., 2.86 g (29.3 mmol) of O,N-dimethyl-hydroxylamine hydrochloride was added and the reaction was stirred overnight at 50° C. Half of the solvent was removed under reduced pressure and the reaction mixture was diluted with 200 mL of cold water. The solids were filtered off, washed with 100 mL of water and dried to give 9.8 g (84%) of the product as a tan powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884110B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-2a00283eae6441d6a0a212ad46728079 |
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| Source note | uspto-grants-2011_02 |
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