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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5730생성일: 2026년 10월 25일

Dicyclohexylcarbodiimide → 1-Benzyloxycarbonyl-4-(N-tert-butoxycarbonyltyrosyl)homopiperazine

https://huagongshe.com/reaction/5730

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물L-Tyrosine, N-(1,1-dimethylethoxy)carbonyl-HCID 117439—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물Benzyl 1,4-diazepane-1-carboxylateHCID 4384955—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyloxycarbonyl-4-(N-tert-butoxycarbonyltyrosyl)homopiperazineHCID 5405993497.7%

반응 단계

15.29 g of N-tert-butoxycarbonyltyrosine and 12.73 g of N-benzyloxycarbonylhomopiperazine were dissolved in 280 ml of tetrahydrofuran, to the solution were added 8.09 g of 1-hydroxybenzotriazole hydrate and 11.77 g of DCC at a room temperature with stirring, and the reaction mixture was stirred for 16 hours. The reaction mixture was evaporated to remove the solvent under a reduced pressure, to the residue was added benzene, and insoluble matter was filtered by suction and washed with benzene. The benzene layers were combined and evaporated off under a reduced pressure. The resulting residue was applied to a silica gel column and eluted with chloroform/methanol (100:1), to obtain 26.42 g of the title compound in colorless amorphous form.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245034
출처 데이터셋uspto-grants-1993_09
ORD IDord-5e959f0c247e4beda9969377311282aa
출처 메모uspto-grants-1993_09