HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Methanesulfonylamino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Amino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazole | HCID 10469982 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methanesulfonylamino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazole | HCID 15676049 | 71% |
Reaction Steps
To a mixture of 2-amino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazole (500 mg, 1.68 mmol) and triethylamine (340 mg, 3.36 mmol) in tetrahydrofuran was added methanesulfonyl chloride (385 mg, 3.36 mmol) by portion and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with water, extracted with ethyl acetate and evaporated under reduced pressure to a residue, which was chromatographed and then recrystallized to afford 2-methanesulfonylamino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazole (447 mg, 71% yield): mp 127.5°-129.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05066666 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-b80f39058228437794815f77022f2f1d |
| Source note | uspto-grants-1991_11 |