戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1940613作成日:2026年10月24日

Triethylamine → N-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-N-phenylglycine methyl ester

https://huagongshe.com/ja/reaction/1940613

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Thionyl ChlorideHCID 24386—
反応物Methyl 2-(phenylamino)acetate hydrochlorideHCID 12241365—
反応物3-(4,5,7-Trifluorobenzothiazol-2-yl)propionic acidHCID 21463529—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物N-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-N-phenylglycine methyl esterHCID 2146350329.4%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05700819
出典データセットuspto-grants-1997_12
ORD IDord-37a26dca2893411c94de2c3f45e583a0
出典メモuspto-grants-1997_12