HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1940613Erstellt: 25. Oktober 2026
Triethylamine → N-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-N-phenylglycine methyl ester
https://huagongshe.com/reaction/1940613
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | Methyl 2-(phenylamino)acetate hydrochloride | HCID 12241365 | — |
| Edukt | 3-(4,5,7-Trifluorobenzothiazol-2-yl)propionic acid | HCID 21463529 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-N-phenylglycine methyl ester | HCID 21463503 | 29,4% |
Reaktionsschritte
To a solution of 3-(4,5,7-trifluorobenzothiazol-2-yl)propionic acid (522 mg, 2 mmol) obtained in Example 3-i) in a mixture of toluene (5 ml) and N,N-dimethylformamide (DMF; 1 ml) was added thionyl chloride (357 mg, 3 mmol) and the mixture was stirred for 1 hour at room temperature. To the ice cold reaction mixture was N-phenylglycine methyl ester hydrochloride (403 mg, 2 mmol) and triethylamine (400 mg, 4 mmol) and the mixture was stirred for 2 hours. The reaction mixture was diluted with water and then extracted with ethyl acetate. The organic layer was washed with water, then dried and evaporated to yield a residue, which was purified on a silica gel column to give N-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-N-phenylglycine methyl ester (240 mg, 29%) as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05700819 |
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| Quelldatensatz | uspto-grants-1997_12 |
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| ORD ID | ord-37a26dca2893411c94de2c3f45e583a0 |
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| Quellennotiz | uspto-grants-1997_12 |
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