돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 876095생성일: 2026년 10월 25일

7-Fluoro-4-nitrobenzo-2-oxa-1,3-diazole → 2-Nbdlg

https://huagongshe.com/reaction/876095

반응식

참여 물질

역할이름HCID투입량
반응물7-Fluoro-4-nitrobenzo-2-oxa-1,3-diazoleHCID 122123—
반응물Sodium BicarbonateHCID 516892—
반응물(3S,4S,5R,6S)-3-amino-6-(hydroxymethyl)oxane-2,4,5-triol;hydrochlorideHCID 45933886—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물2-NbdlgHCID 87308104—

반응 조건

온도37 °C

반응 단계

In a brown flask, L-glucosamine hydrochloride (40.0 mg) and NaHCO3 (26.0 mg) were placed and dissolved in water (800 μl). A solution in which 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F) (92.0 mg) was dissolved in methanol (4.0 ml) was added thereto, and under an argon atmosphere, the resulting mixture was stirred for 2 hours at a bath temperature of 37° C. Thereafter, the mixture was stirred at room temperature for an additional 40 minutes. Methanol was removed by concentration under reduced pressure, and the resulting precipitates (unnecessary substances derived from NBD-F) were removed by filtration. The precipitates were washed with water, and the filtrate and the washing solution were combined, followed by purification by HPLC. A target fraction was collected and lyophilized, whereby a target product was obtained (yield: 48.7 mg, yield ratio: 76%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08986656B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-f6c1e9a5909b4aae9c96477c7f1ebd69
출처 메모uspto-grants-2015_03