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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 459653생성일: 2026년 10월 24일

Chloroform → N-([1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]methyl}-N-[2-(tritylamino)ethyl]guanidine

https://huagongshe.com/ko/reaction/459653

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물Trityl chlorideHCID 6456—
반응물N-[(5-amino-1-methyl-1H-pyrazol-4-yl)methyl]-N',N''-bis(tert-butoxycarbonyl)-N-[2-(tritylamino)ethyl]guanidineHCID 68519459—
용매PyridineHCID 1049—
생성물N-([1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]methyl}-N-[2-(tritylamino)ethyl]guanidineHCID 8676045981.7%

반응 단계

To a solution of N-[(5-amino-1-methyl-1H-pyrazol-4-yl)methyl]-N′,N″-bis(tert-butoxycarbonyl)-N-[2-(tritylamino)ethyl]guanidine (1.84 g) in pyridine (10 ml) was added triphenylmethyl chloride (0.94 g), and the mixture was stirred at room temperature for 3 hours. To the reaction mixture was added chloroform (50 ml). The mixture was washed successively with 10% aqueous citric acid solution, brine and saturated aqueous sodium hydrogencarbonate solution. 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′,N″-bis(tert-butoxycarbonyl{-N-([1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]methyl}-N-[2-(tritylamino)ethyl]guanidine (1.60 g) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07192943B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-f72b8e94ca8348b2b6cd4309decc6194
출처 메모uspto-grants-2007_03