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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 440127생성일: 2026년 10월 24일

2-(6-(Bis(carboxymethyl)amino)-5-(2-(2-(bis(carboxymethyl)amino)-5-methylphenoxy)ethoxy)-2-benzofuranyl)-5-oxazolecarboxylic acid → Fura F

https://huagongshe.com/ko/reaction/440127

반응식

참여 물질

역할이름HCID투입량
반응물2-(6-(Bis(carboxymethyl)amino)-5-(2-(2-(bis(carboxymethyl)amino)-5-methylphenoxy)ethoxy)-2-benzofuranyl)-5-oxazolecarboxylic acidHCID 57054—
반응물Proton spongeHCID 88675—
반응물BaptaHCID 104751—
반응물2,3-Difluoro-6-nitrophenolHCID 2733745—
반응물N,N'-[1,2-Ethanediylbis[oxy(4-fluoro-2,1-phenylene)]]bis[N-(carboxymethyl)glycine]HCID 11027644—
생성물Fura FHCID 3025888—

반응 단계

As discussed above, the synthesis of 5,5', 6,6'-tetrafluoro-BAPTA (Formula II) was carried out as originally described for both BAPTA and 5,5'-difluoro BAPTA starting from commercially available 2-nitro-5,6-difluorophenol. Fura-F was synthesized via the pathway originally described for the preparation of Fura-2. Unless otherwise noted commercially available reagents and dry solvents were used as received. Reactions were carried out under an atmosphere of argon and reaction temperatures refer to the bath. Flash column chromatography was performed with Merck Silica Gel 60 (40-63 μm). Proton sponge is 1,8-bis(dimethylamino)naphthalene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05516911
출처 데이터셋uspto-grants-1996_05
ORD IDord-76d2846edae443ab9eed0f43a815ffed
출처 메모uspto-grants-1996_05