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HRID 1951421생성일: 2026년 10월 25일

Methanol → 4-(3-Acetyl-5-ethoxy-2-methyl-1,4-dihydro-1,6-naphthyridin-4-yl)-1-naphthonitrile

https://huagongshe.com/reaction/1951421

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물DichloromethaneHCID 6344—
반응물Triethyloxonium tetrafluoroborateHCID 2723982—
반응물4-(3-Acetyl-2-methyl-5-oxo-1,4,5,6-tetrahydro-1,6-naphthyridin-4-yl)-1-naphthonitrileHCID 59603025—
용매WaterHCID 962—
생성물4-(3-Acetyl-5-ethoxy-2-methyl-1,4-dihydro-1,6-naphthyridin-4-yl)-1-naphthonitrileHCID 23627989—

반응 단계

93 mg (0.262 mmol) of 4-(3-acetyl-2-methyl-5-oxo-1,4,5,6-tetrahydro-1,6-naphthyridin-4-yl)-1-naphthonitrile are dissolved under an argon atmosphere in 5 ml of abs. dichloromethane, and 99.4 mg (0.268 mmol) of triethyloxonium tetrafluoroborate are added. After a reaction time of two hours at room temperature (reaction checked by HPLC), the mixture is mixed with 5 ml of methanol and 0.5 ml of water and again stirred for 2 h. It is then diluted with 20 ml of water and extracted three times with dichloromethane. The combined organic phases are dried with sodium sulfate, and the solvent is removed in a rotary evaporator. The residue is purified by preparative HPLC (eluent: acetonitrile/water with 0.1% formic acid, gradient 20:80→95:5). 60 mg (59.8% of theory) of the title compound are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08404709B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-fe52c5d155c844f0a03dcff3b06b4614
출처 메모uspto-grants-2013_03