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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75410생성일: 2026년 10월 23일

Triethylamine → 3-(2,6-Dichloro-pyrimidin-4-yl)-8-oxa-3-aza-bicyclo[3.2.1]octane

https://huagongshe.com/ko/reaction/75410

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,4,6-TrichloropyrimidineHCID 77378—
반응물8-Oxa-3-aza-bicyclo(3.2.1)octane hydrochlorideHCID 21983536—
용매EthanolHCID 702—
생성물3-(2,6-Dichloro-pyrimidin-4-yl)-8-oxa-3-aza-bicyclo[3.2.1]octaneHCID 8666587983%
생성물3-(4,6-Dichloro-pyrimidin-2-yl)-8-oxa-3-aza-bicyclo[3.2.1]octaneHCID 8666588011%

반응 단계

2,4,6-Trichloropyrimidine (8, 6.325 mL, 55 mmol) was dissolved in 220 mL EtOH at 0° C. 8-Oxa-3-aza-bicyclo[3.2.1]octane hydrochloride (2, 8.23 g, 55 mmol) was added followed by the addition of NEt3 (23.1 mL, 165 mmol). The mixture was allowed to warm to room temperature and stirred for 1 hour at ambient temperature. The mixture was concentrated, dissolved in EtOAc and washed with saturated NaHCO3. The aqueous phase was extracted with EtOAc the combined organic phases were dried (MgSO4), filtered, and concentrated. The mixture was purified by silica gel chromatography (10-80% EtOAc in hexanes) to give 11.807 g (45 mmol, 83%) of 3-(2,6-dichloro-pyrimidin-4-yl)-8-oxa-3-aza-bicyclo[3.2.1]octane (9) along with 1.631 g (6.2 mmol, 11%) of 3-(4,6-dichloro-pyrimidin-2-yl)-8-oxa-3-aza-bicyclo[3.2.1]octane (10).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835429B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-7ccd338c5fbb421d822032d9cc5cadba
출처 메모uspto-grants-2014_09