Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276858생성일: 2026년 10월 25일
Trifluoroacetic acid → 6-Amino-4-(3-bromo-phenylamino)-[1,7]naphthyridine-3-carbonitrile
https://huagongshe.com/reaction/276858
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | 4-Methoxybenzylamine | HCID 75452 | — |
| 반응물 | 4-(3-Bromo-phenylamino)-6-fluoro-[1,7]naphthyridine-3-carbonitrile | HCID 18548979 | — |
| 반응물 | Chloroform methanol | HCID 21584188 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 6-Amino-4-(3-bromo-phenylamino)-[1,7]naphthyridine-3-carbonitrile | HCID 9798006 | — |
반응 단계
To 1.3 g of 4-(3-bromo-phenylamino)-6-fluoro-[1.7]naphthyridine-3-carbonitrile in 20 mL of absolute ethanol was added 5 ml of 4-methoxy-benzylamine. The reaction was refluxed for six days, stripped of solvents, and passed through a plug of silica gel with 5% methanol/chloroform. This crude product was dissolved in 10 mL of chloroform containing 5% anisole and 10 mL of trifluoroacetic acid was added. After stirring under an inert atmosphere for 20 hours, 10 mL of toluene was added and the solvents stripped on a rotary evaporator. The product was purified by flash chromatography with a gradient of 0-10% methanol/chloroform. The solid was extracted with hot, 5% methanol/isopropyl ether and then cooled, filtered, and dried to give 250 mg of 6-amino-4-(3-bromo-phenylamino)-[1.7]naphthyridine-3-carbonitrile as an off-white solid. mass spectrum (m/e): M+H 306.2.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06355636B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-6d2ad1b6640247b58f8e221f0e4a0ebf |
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| 출처 메모 | uspto-grants-2002_03 |
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