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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197434Generated: October 31, 2026

N-Methylpiperidine → N-methyl-N-methoxy-2-chloro-5-sulfamoylthiophene-3-carboxamide

https://huagongshe.com/reaction/1197434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylpiperidineHCID 12291—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Chloro-5-sulfamoylthiophene-3-carboxylic acidHCID 1201498—
SolventDimethylformamideHCID 6228—
ProductN-methyl-N-methoxy-2-chloro-5-sulfamoylthiophene-3-carboxamideHCID 1910647840.4%

Reaction Steps

1,1-Carbonyldiimidazole (7.70 g, 0.047 mol) was added portionwise to a solution of 5-chloro-4-carboxythiophene-2-sulfonamide (7.25 g, 0.03 mol) in DMF (60 mL). After two hours, N-methylpiperidine (6.0 mL, 0.05 mol) and N,O-dimethylhydroxylamine hydrochloride (5.2 g, 0.05 mol) were added to the reaction mixture. After an additional four hours at room temperature, the reaction mixture was poured into ice/water saturated with NaHCO3. The crude product was extracted into ethyl acetate, the extract was dried (anhydrous Na2SO4), filtered and evaporated. The crude residue was chromatographed on silica gel and eluted with 59% methanol/methylene chloride to give 3.45 g (40%) of white solid product, mp 223°-225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05276025
Source datasetuspto-grants-1994_01
ORD IDord-1cc4ccf734414bdb81426a48f463ec72
Source noteuspto-grants-1994_01