HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Aminosulfonyl)-4-chlorobenzoyl chloride → 4-Chloro-N-[4-(2-methoxyphenyl)-1-piperazinyl]-3-sulfamoylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Aminosulfonyl)-4-chlorobenzoyl chloride | HCID 3017979 | — |
| Reactant | 4-(2-Methoxyphenyl)piperazin-1-amine | HCID 13730200 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-Chloro-N-[4-(2-methoxyphenyl)-1-piperazinyl]-3-sulfamoylbenzamide | HCID 13730201 | — |
Reaction Steps
To a mixture of 1 g of 1-amino-4-(2-methoxyphenyl)piperazine and 1 ml of triethylamine was added 1.25 g of 4-chloro-3-sulfamoylbenzoyl chloride under stirring at room temperature. The reaction mixture was stirred at room temperature for 9 hours. The resulting precipitate was filtered, washed with water and recrystallized from ethanol to afford a title compound in a yield of 1.20 g (60%) as colorless needle crystals, mp 231°-233° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04650871 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-940e105c96124fa69662da1fd4464f7d |
| Source note | uspto-grants-1987_03 |