HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-[2-[4-[(Methylsulfonyl)amino]phenyl]ethyl]-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-[2-(1H-imidazol-1-yl)ethyl]aniline | HCID 3523674 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[2-[4-[(Methylsulfonyl)amino]phenyl]ethyl]-1H-imidazole | HCID 13763397 | — |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
To a -10° C. solution of 8 g (0.064 mole) of 1-[2-(4-aminophenyl)ethyl]-1H-imidazole and 10 mL triethylamine in 200 mL of methylene chloride add 5 mL of methanesulfonyl chloride dropwise. Stir the resulting solution at -10° C. for about 30 minutes then warm to ambient temperature for about 30 minutes. Wash the reaction mixture with water (2×100 mL). Extract with 10% aqueous sodium hydroxide (2×50 mL). The combined aqueous extracts are neutralized with ammonium chloride then extracted with methylene chloride (2×100 mL) and combined. Remove the solvent in vacuo to provide the title compound, which may be recrystallized from tetrahydrofuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04689341 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-cd66aca946ca4ec298c6a1d5a5a8d280 |
| Source note | uspto-grants-1987_08 |