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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 459652생성일: 2026년 10월 24일

Triethylamine → N-[(5-amino-1-methyl-1H-pyrazol-4-yl)methyl]-N',N''-bis(tert-butoxycarbonyl)-N-[2-(tritylamino)ethyl]guanidine

https://huagongshe.com/ko/reaction/459652

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidineHCID 3694570—
반응물N-[(5-amino-1-methyl-1H-pyrazol-4-yl)methyl]-N'-tritylethane-1,2-diamineHCID 18442411—
용매ChloroformHCID 6212—
생성물N-[(5-amino-1-methyl-1H-pyrazol-4-yl)methyl]-N',N''-bis(tert-butoxycarbonyl)-N-[2-(tritylamino)ethyl]guanidineHCID 6851945925.2%

반응 단계

To a solution of N-[(5-amino-1-methyl-1H-pyrazol-4-yl)methyl]-N′-tritylethane-1,2-diamine (7.50 g) and triethylamine (2.86 g) in chloroform (100 ml) was added di-tert-butyl ({[(trifluoromethyl)sulfonyl]imino}-methylene)biscarbamate (11.05 g). The mixture was stirred at room temperature for 4 days. The reaction mixture was washed successively with 10% aqueous citric acid solution and brine, and the organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with 3% methanol/chloroform to give N-[(5-amino-1-methyl-1H-pyrazol-4-yl)methyl]-N′,N″-bis(tert-butoxycarbonyl)-N-[2-(tritylamino)ethyl]guanidine (3.00 g) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07192943B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-25b47db223204645b643fcf71cdc9cd0
출처 메모uspto-grants-2007_03