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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51340생성일: 2026년 10월 23일

Sulfuric Acid → 5-(2-Amino)ethyloxy-9-benzyl-7-methoxy-1,2,3,4-tetrahydrocarbazole-4-carboxamide

https://huagongshe.com/ko/reaction/51340

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물9-Benzyl-7-methoxy-5-cyanomethyloxy-1,2,3,4-tetrahydrocarbazole-4-carboxamideHCID 10134925—
반응물lithium aluminium hydride THFHCID 68718528—
용매TetrahydrofuranHCID 8028—
생성물5-(2-Amino)ethyloxy-9-benzyl-7-methoxy-1,2,3,4-tetrahydrocarbazole-4-carboxamideHCID 2273913255.2%

반응 단계

To 1.93 ml (1.93 mmol) 1M lithium aluminum hydride/THF in 13 ml THF at 0° C. was added H2SO4(53 μl, 0.97 mmol) dropwise over 5 min. The mixture was allowed to stir at room temperature 1 hour, then a solution of 9-benzyl-7-methoxy-5-cyanomethyloxy-1,2,3,4-tetrahydrocarbazole-4-carboxamide (0.50 g, 1.29 mmol) in 13 ml THF was added dropwise at a rate which kept the temperature below 26° C. After an additional 45 minutes, the reaction was quenched with 0.5 ml 1:1 THF/H2O, 0.75 ml 13% NaOH, and finally 80 μl H2O. The reaction was diluted with EtOAc and saturated NaHCO3, and the layers separated. The organic layer was extracted with brine, dried over sodium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel eluting with 9:1:0.1 CH2Cl2/MeOH/NH4OH to give the subtitled product (0.28 g, 55%). MS (ES+) 394

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713645B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-b3c0a4b14992469eaa6f497fccc83053
출처 메모uspto-grants-2004_03