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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktThionyl ChlorideHCID 24386—
EduktMethyl 2-(phenylamino)acetate hydrochlorideHCID 12241365—
Edukt3-(4,5,7-Trifluorobenzothiazol-2-yl)propionic acidHCID 21463529—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-N-phenylglycine methyl esterHCID 2146350329,4%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05700819
Quelldatensatzuspto-grants-1997_12
ORD IDord-37a26dca2893411c94de2c3f45e583a0
Quellennotizuspto-grants-1997_12