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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25114생성일: 2026년 10월 26일

Benzylamine → N,N'-Dicyclohexylurea

https://huagongshe.com/reaction/25114

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
용매AcetonitrileHCID 6342—
생성물N,N'-DicyclohexylureaHCID 4277—

반응 단계

Fmoc-arginine(PMC)—OH AA3 (3.83 g, 5.0 mmol) and HOBT (0.76 g, 5.0 mmol) were combined in acetonitrile (100 mL) and benzylamine (0.54 g, 5.0 mmol) was added dropwise at about rt, followed by DCC (2.06 g, 10.0 mmol) and stirred for about 16 h. A solid was filtered and the filtrate was evaporated in vacuo to an oil, which was then dissolved in ethyl acetate (100 mL) and washed with saturated NaHCO3 (2×), brine (2×), then dried (Na2SO4) and evaporated in vacuo to a solid, which was triturated with hexane (2×) to give a solid (impure with dicyclohexylurea). A portion of this solid (1.17 g, 1.25 mmol) was dissolved in acetonitrile (30 mL), diethyl amine (1.5 mL) was added and the reaction was stirred at about rt for about 1 h. The solution was then evaporated in vacuo to a solid, which was triturated with hexane (2×). The solution was then evaporated in vacuo to a solid, which was then combined in ACN (25 mL) with Fmoc-3,4difluorophenylalanine (0.53 g, 1.25 mmol) and HOBT (0.19 g, 1.25 mmol). DIC (0.32 g, 2.5 mmol) was added and the reaction was stirred at about rt for about 16 h. Fmoc-protected dipeptide was filtered (0.77 g) and stirred in ACN (30 mL) with diethyl amine (1.5 mL) for about 2.5 h. The reaction was evaporated in vacuo to an oil, which was triturated with hexane (3×) to the white solid AA4.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858577B1
출처 데이터셋uspto-grants-2005_02
ORD IDord-c8850f81b56d4459b3d879b72986bc97
출처 메모uspto-grants-2005_02