HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352241Generated: October 26, 2026
Potassium Iodide → 4-Methylsulfonylaminobenzoyl-1-[3-(4-pyridyl)-propyl]piperidine dihydrochloride
https://huagongshe.com/reaction/2352241
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Pyridine, 4-(3-chloropropyl)-, hydrochloride | HCID 205441 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-[4-(piperidine-4-carbonyl)-phenyl]methanesulfonamide hydrochloride | HCID 14130042 | — |
| Product | 4-Methylsulfonylaminobenzoyl-1-[3-(4-pyridyl)-propyl]piperidine dihydrochloride | HCID 86743470 | 66% |
Reaction Steps
0.295 g (0.926 mmol) of 4-(4-methylsulfonylaminobenzoyl)piperidine hydrochloride and 0.380 g (4.52 mmol) of sodium hydrogencarbonate were suspended in 4 ml of dimethylformamide and the suspension was stirred at 85° C. for 40 min. 0.20 g (1.04 mmol) of 4-(3-chloropropyl)pyridine hydrochloride and 0.31 g (1.87 mmol) of potassium iodide were added to the suspension and the mixture was stirred at 85° C. for 1.5 h. The liquid reaction mixture was filtered and the filtrate was concentrated. The obtained residue was purified according to silica gel column chromatography (chloroform:methanol:aqueous ammonia=96:4:0.4). The purified product was converted into its hydrochloride with ethanolic hydrogen chloride and recrystallized from ethanol to obtain 0.288 g (66%) of the intended compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04876262 |
|---|
| Source dataset | uspto-grants-1989_10 |
|---|
| ORD ID | ord-d7b12f61fb6940d1bc62984f20a4cd13 |
|---|
| Source note | uspto-grants-1989_10 |
|---|