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HRID 581180作成日:2026年10月26日

N-(tert-butoxycarbonyl)glycine → N-(2-Benzyloxyphenyl)-2-(N-tertiary butoxycarbonylamino)acetamide

https://huagongshe.com/reaction/581180

反応式

関与物質

役割名称HCID仕込み量
反応物N-(tert-butoxycarbonyl)glycineHCID 78288—
反応物2-BenzyloxyanilineHCID 240548—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物N-(2-Benzyloxyphenyl)-2-(N-tertiary butoxycarbonylamino)acetamideHCID 1076072139.3%

反応手順

2-Benzyloxyaniline (S1) (16.4 g), 4-dimethylamino-pyridine (11.0 g), and N-tertiarybutoxycarbonylglycine (14.4 g) were dissolved in dichloromethane. To the resulting solution, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (16.3 g) was added and stirred for 12 hours at room temperature. The reaction mixture was washed -successively with 1N HCl, saturated aqueous sodium hydrogencarbonate solution and brine, then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, obtaining 11.5 g of the compound S2 as white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05919824
出典データセットuspto-grants-1999_07
ORD IDord-b44b8e5944b745e288b15e69b0db9131
出典メモuspto-grants-1999_07