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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52941생성일: 2026년 10월 24일

N-Hydroxysuccinimide → Succinimido 1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-4-hydroxymethylimidazole-5-carboxylate

https://huagongshe.com/ko/reaction/52941

반응식

참여 물질

역할이름HCID투입량
반응물N-HydroxysuccinimideHCID 80170—
반응물1-[(2'-t-Butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-4-hydroxymethylimidazole-5-carboxylic acidHCID 19036119—
용매TetrahydrofuranHCID 8028—
생성물Succinimido 1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-4-hydroxymethylimidazole-5-carboxylateHCID 1903623992.7%

반응 단계

206 mg of N,N-dicyclohexylcarbodiimide were added to a suspension of 464 mg of 1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-4-hydroxymethylimidazole-5-carboxylic acid (prepared as described in Example 4) and 140 mg of N-hydroxysuccinimide in 10 ml of tetrahydrofuran, and the resulting mixture was stirred at room temperature for 16 hours. At the end of this time, the material which had precipitated was filtered off and the filtrate was concentrated by evaporation under reduced pressure. The concentrate was purified by column chromatography through silica gel, using a 1:15 by volume mixture of methanol and methylene chloride as the eluent, to afford 0.52 g of the title compound as crystals, melting at 107°-109° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616599
출처 데이터셋uspto-grants-1997_04
ORD IDord-9fb028dd2b564ff38d2d7769381c477e
출처 메모uspto-grants-1997_04