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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054504Generated: October 30, 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/1054504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantHCID 57870807HCID 57870807—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Chloro-3-trifluoromethyl-benzenesulfonylamino)-5-methyl-pyridine-2-carboxylic acid methoxy-methyl-amideHCID 5787080884.1%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394307B2
Source datasetuspto-grants-2016_07
ORD IDord-a1f4fdee62f2441bb07922e0e6586a1f
Source noteuspto-grants-2016_07