돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75440생성일: 2026년 10월 24일

Triethylamine → 3-(2,6-Dichloro-5-nitropyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octane

https://huagongshe.com/ko/reaction/75440

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,4,6-Trichloro-5-nitropyrimidineHCID 4297843—
반응물8-Oxa-3-aza-bicyclo(3.2.1)octane hydrochlorideHCID 21983536—
용매DichloromethaneHCID 6344—
생성물3-(2,6-Dichloro-5-nitropyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octaneHCID 86665896—

반응 조건

온도0 °C

반응 단계

2,4,6-Trichloro-5-nitropyrimidine (45, 1.43 g, 6.26 mmoles) was dissolved in dichloromethane and cooled to 0° C. A solution of 8-oxa-3-azabicyclo[3.2.1]octane (2, 0.934 g, 6.26 mmoles) in dichloromethane and triethylamine (0.873 mL, 6.26 mmoles) was slowly added over 1 hour. The solution was allowed to stir at 0° C. for 2 hours, then warmed to room temperature and stirred for an additional 16 hours. The reaction mixture was filtered, the filtrate was concentrated, dissolved in ethyl acetate, washed with 1N hydrochloric acid, saturated sodium bicarbonate, brine, dried, and concentrated to provide 3-(2,6-dichloro-5-nitropyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octane (46). Yield: 1.53 g (80%). HRMS; [M+H]+ Obs'd=305.0200, [M+H]+ Calc'd=305.0203.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835429B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-7de2637b233449baa3af76c79335ccfc
출처 메모uspto-grants-2014_09