HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylpiperidine → N-methyl-N-methoxy-2-chloro-5-sulfamoylthiophene-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylpiperidine | HCID 12291 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Chloro-5-sulfamoylthiophene-3-carboxylic acid | HCID 1201498 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-methyl-N-methoxy-2-chloro-5-sulfamoylthiophene-3-carboxamide | HCID 19106478 | 40.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05276025 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-1cc4ccf734414bdb81426a48f463ec72 |
| Source note | uspto-grants-1994_01 |