HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzenesulfonyl chloride → 2-(4-chlorobenzenesulphonamido)-N-(3-imidazol-1-ylpropyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-amino-N-(3-imidazol-1-ylpropyl)benzamide | HCID 2798335 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-chlorobenzenesulphonamido)-N-(3-imidazol-1-ylpropyl)benzamide | HCID 2798336 | 45.4% |
Reaction Steps
4-Chlorobenzenesulphonyl chloride (1.56 g) was added in portions over 2 minutes to a solution of 2-amino-N-(3-imidazol-1-ylpropyl)benzamide (1.8 g) in water (50 ml) at 80° C. on a steam bath. The mixture was stirred at 80°-90° C. for 3 hours, cooled to room temperature and brought to pH 7 with saturated aqueous sodium bicarbonate solution. The crude product which had precipitated was extracted into dichloromethane (2×100 ml); the resulting solution was dried over magnesium sulphate and evaporated to give a solid. The solid was recrystallised from ethanol to give 2-(4-chlorobenzenesulphonamido)-N-(3-imidazol-1-ylpropyl)benzamide (1.4 g), in the form of a white solid, m.p. 174°-176° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04507315 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-6238ef570f9e42dd95371431c4a2d662 |
| Source note | uspto-grants-1985_03 |