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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 598036생성일: 2026년 10월 25일

Triethylamine → 1-{[(7-Bromo-3-nitro[1,5]naphthyridin-4-yl)amino]methyl}cyclopentanol

https://huagongshe.com/reaction/598036

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-(Aminomethyl)cyclopentan-1-olHCID 13051202—
반응물7-Bromo-4-chloro-3-nitro[1,5]naphthyridineHCID 57457837—
용매ChloroformHCID 6212—
생성물1-{[(7-Bromo-3-nitro[1,5]naphthyridin-4-yl)amino]methyl}cyclopentanolHCID 67052453—

반응 조건

온도0 °C

반응 단계

A suspension of 7-bromo-4-chloro-3-nitro[1,5]naphthyridine (54.42 g, 188.6 mmol) in chloroform (820 mL) was cooled to 0° C., and triethylamine (105 mL, 755 mmol) was added. A solution of 1-(aminomethyl)cyclopentanol (28.25 g, 245.2 mmol) in chloroform (272 mL) was added slowly over a period of 15 minutes. The reaction was allowed to warm to room temperature and stirred for 30 minutes. The solution was washed sequentially with water (500 mL) and saturated aqueous sodium bicarbonate (750 mL), dried over sodium sulfate, filtered, and concentrated under reduced pressure to provide 1-{[(7-bromo-3-nitro[1,5]naphthyridin-4-yl)amino]methyl}cyclopentanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07897609B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-c3aa6b0b83bb485ca8fb2bfacae7a3f6
출처 메모uspto-grants-2011_03