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HRID 34052作成日:2026年10月24日

Benzyl carbazate → N'-[2-(tert-Butoxycarbonyl-methyl-amino)-acetyl]-hydrazine Carboxylic Acid Benzyl Ester

https://huagongshe.com/ja/reaction/34052

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl carbazateHCID 79242—
反応物DiisopropylethylamineHCID 81531—
反応物Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-HCID 83692—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物N'-[2-(tert-Butoxycarbonyl-methyl-amino)-acetyl]-hydrazine Carboxylic Acid Benzyl EsterHCID 5979692188%

反応手順

6.95 g of 2-(tert-butoxycarbonyl-methyl-amino)-acetic acid, 6.1 g of hydrazine carboxylic acid benzyl ester, 6.18 g of 1-hydroxybenzotriazole monohydrate and 19.2 mL of N,N-diisopropylethylamine were dissolved in 120 mL of N,N-dimethylformamide, and 10.6 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added under stirring at room temperature. After stirring at room temperature for 17 hours, the reaction solution was added with water and extracted with ethyl acetate, and the resultant organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was evaporated, followed by purification by silica gel column chromatography (hexane:ethyl acetate=1:1), to obtain 10.9 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429609B2
出典データセットuspto-grants-2008_09
ORD IDord-7308ab218bc44c31ba569428a619ac05
出典メモuspto-grants-2008_09