HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-[2-(4,5,7-trifluorobenzothiazol-2-ylthio)acetyl]-N-phenylglycine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Calcium Carbonate | HCID 10112 | — |
| Reactant | N-chloroacetyl-N-phenylglycine methyl ester | HCID 21463537 | — |
| Reactant | HCID 178505914 | HCID 178505914 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[2-(4,5,7-trifluorobenzothiazol-2-ylthio)acetyl]-N-phenylglycine methyl ester | HCID 21463552 | 82.1% |
Reaction Steps
To dimethylsulfoxide (DMSO; 6 ml) was added 4,5,7-trifluoro-2-mercaptobenzothiazole (442 mg, 2 mmol), N-chloroacetyl-N-phenylglycine methyl ester (479 mg, 2 mmol), calcium carbonate (276 mg, 2 mmol) and potassium iodide (20 mg) and the mixture was stirred at room temperature for 1 hour. The resultant reaction mixture was diluted with water, acidified with 7% hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water, dried and then evaporated to yield a residue, which was crystallized from isopropyl ether to give N-[2-(4,5,7-trifluorobenzothiazol-2-ylthio)acetyl]-N-phenylglycine methyl ester (700 mg, 82%) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05700819 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-39e246432cb740bca20fe38fef52d529 |
| Source note | uspto-grants-1997_12 |