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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 370271생성일: 2026년 10월 24일

Xanthene-9-carboxylic acid → N-[9-(cyclooctylmethyl)-9-azabicyclo[3.3.1]nonan-3-yl]xanthene-9-carboxamide

https://huagongshe.com/ko/reaction/370271

반응식

참여 물질

역할이름HCID투입량
반응물Xanthene-9-carboxylic acidHCID 65736—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물Tert-butyl 3-amino-9-azabicyclo[3.3.1]nonane-9-carboxylateHCID 23283006—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-[9-(cyclooctylmethyl)-9-azabicyclo[3.3.1]nonan-3-yl]xanthene-9-carboxamideHCID 1548066992.9%

반응 단계

15 ml of anhydrous N,N-dimethylformamide suspension having 165 mg of 3-amino-9-t-butoxycarbonyl-9-azabicyclo[3.3.1]nonane and 155 mg of xanthene-9-carboxylic acid was cooled with ice, and 224 mg of EDCI.HCl and 157 mg of 1-hydroxybenzotriazole were successively added thereto. The temperature was raised to room temperature immediately, and the reaction mixture was stirred for 21 hours. 10 ml of water was added to the reaction solution, followed by extraction with diethyl ether. The organic layer was washed with 10% citric acid solution, saturated aqueous sodium bicarbonate, water and saturated aqueous sodium chloride, followed by drying over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and 301 mg of the title compound as a white solid was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06140338
출처 데이터셋uspto-grants-2000_10
ORD IDord-37a5a51b4e0a4336a8ee8e83cf8c5826
출처 메모uspto-grants-2000_10