HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → N-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-N-methylglycine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-N-methylglycine ethyl ester | HCID 21463533 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-N-methylglycine | HCID 21463526 | 70% |
Reaction Steps
To a solution of N-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-N-methylglycine ethyl ester (290 mg, 0.8 mmol) in methanol (2 ml) was added 2N sodium hydroxide (0.5 ml, 1 mmol) and the mixture was stirred for 30 min. at room temperature. The reaction mixture was diluted with water and then washed with ether. The aqueous layer was acidified with 7% hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water, then dried and evaporated to yield a residue, which was recrystallized from ethanol-isopropyl ether to give N-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-N-methylglycine (185 mg, 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05700819 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-7e6977eeb76b461c8369f188539c303c |
| Source note | uspto-grants-1997_12 |