Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| 반응물 | 4-(3-Acetyl-2-methyl-5-oxo-1,4,5,6-tetrahydro-1,6-naphthyridin-4-yl)-1-naphthonitrile | HCID 59603025 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-(3-Acetyl-5-ethoxy-2-methyl-1,4-dihydro-1,6-naphthyridin-4-yl)-1-naphthonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08404709B2 |
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| 출처 데이터셋 | uspto-grants-2013_03 |
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| ORD ID | ord-fe52c5d155c844f0a03dcff3b06b4614 |
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| 출처 메모 | uspto-grants-2013_03 |
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