HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-[(2-Sulfamoyl-5-thienyl)sulfonyl]phenyl 1-acetylpiperidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(4-Hydroxyphenyl)sulfonylthiophene-2-sulfonamide | HCID 12736892 | — |
| Reactant | 1-Acetylpiperidine-4-carbonyl chloride hydrochloride | HCID 53430810 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-[(2-Sulfamoyl-5-thienyl)sulfonyl]phenyl 1-acetylpiperidine-4-carboxylate | HCID 20442367 | — |
Reaction Steps
A solution of 5-[(4-hydroxyphenyl)sulfonyl]thiophene-2-sulfonamide (3.19 g; 0.01 mole) in acetone (60 ml) at -15° was treated with triethylamine (1.11 g; 0.011 mole). Then 1-acetylpiperidine-4-carbonyl chloride hydrochloride (2.41 g; 0.011 mole) was added, portionwise, during 15 minutes at -15°. The cooling bath was removed and stirring was continued. After 20 hours at room temperature, the reaction mixture was treated with triethylamine (1.11 g; 0.011 mole). Then after stirring one hour longer, the reaction mixture was treated with 1-acetylpiperidine-4-carbonyl chloride hydrochloride (2.41 g; 0.011 mole) and triethylamine (2.22 g; 0.022 mole) and stirred at room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04477466 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-d259bbaad2a743b2b218fca536653630 |
| Source note | uspto-grants-1984_10 |