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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34052생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl carbazateHCID 79242—
반응물DiisopropylethylamineHCID 81531—
반응물Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-HCID 83692—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N'-[2-(tert-Butoxycarbonyl-methyl-amino)-acetyl]-hydrazine Carboxylic Acid Benzyl EsterHCID 5979692188%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429609B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-7308ab218bc44c31ba569428a619ac05
출처 메모uspto-grants-2008_09