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HRID 1940611作成日:2026年10月25日

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

https://huagongshe.com/reaction/1940611

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl N-methylaminoacetate hydrochlorideHCID 171173—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物3-(4,5,7-Trifluorobenzothiazol-2-yl)propionic acidHCID 21463529—
溶媒DichloromethaneHCID 6344—
生成物N-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-N-methylglycine ethyl esterHCID 2146353385%

反応手順

To methylene chloride (10 ml) was added sarcosine ethyl ester hydrochloride (307 mg, 2 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (WSC.HCl; 422 mg, 2.2 mmol), 3-(4,5,7-trifluorobenzothiazol-2-yl)propionic acid (522 mg, 2 mmol) and triethylamine (220 mg, 2.2 mmol), and the mixture was stirred at room temperature for 15 hours. The resulting mixture was washed with water, 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-methylglycine ethyl ester (610 mg, 85%) 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-ff383a306367473ba5c1ae34e4d81aa7
出典メモuspto-grants-1997_12