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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1247798생성일: 2026년 10월 26일

N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide ester → 5-Amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazole

https://huagongshe.com/reaction/1247798

반응식

참여 물질

역할이름HCID투입량
반응물N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide esterHCID 76926—
반응물DiisopropylethylamineHCID 81531—
반응물4,5-Diamino-1-(2-hydroxyethyl)pyrazole sulfateHCID 11673148—
용매DichloromethaneHCID 6344—
생성물5-Amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazoleHCID 2190451580.8%

반응 단계

To a suspension of 4,5-diamino-1-(2-hydroxyethyl)pyrazole sulfuric acid salt (1.20 g) and N-[2-(tert-butoxycarbonylamino)acetoxy]succinimide (1.35 g) in methylene chloride (20 ml) was added N-ethyldiisopropylamine (2.1 ml) under ice-cooling, and the mixture was stirred at room temperature for 17 hours. The reaction mixture was washed with water (40 ml), saturated aqueous sodium hydrogen carbonate solution (40 ml) and brine (40 ml). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The oily residue was purified by column chromatography on silica gel eluting with 10% methanol/chloroform to give 5-amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazole (1.20 g) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07129232B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-52dd1d3126c343a9b2cb3cf6af9914c6
출처 메모uspto-grants-2006_10