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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75408생성일: 2026년 10월 24일

Triethylamine → 3-(2-Chloropyrimidin-4-yl)-8-oxa-3-azabicyclo[3,2,1]octane

https://huagongshe.com/ko/reaction/75408

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,4-DichloropyrimidineHCID 77531—
반응물8-Oxa-3-aza-bicyclo(3.2.1)octane hydrochlorideHCID 21983536—
용매EthanolHCID 702—
생성물3-(2-Chloropyrimidin-4-yl)-8-oxa-3-azabicyclo[3,2,1]octaneHCID 6637152789%
생성물3-(4-Chloro-pyrimidin-2-yl)-8-oxa-3-aza-bicyclo[3.2.1]octaneHCID 866658784%

반응 단계

A 745 mg (5 mmol) portion 2,4-dichloropyrimidine (1) was dissolved in 20 mL EtOH at 0 C. 8-oxa-3-aza-bicyclo[3.2.1]octane hydrochloride (2, 748 mg, 5 mmol) was added followed by the addition of NEt3 (2.1 mL, 15 mmol). The mixture was 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 and the combined organic phases were dried (MgSO4), filtered and concentrated. The mixture was purified by silica gel chromatography (20-70% EtOAc in hexanes) to give 1,003 mg (4.4 mmol, 89%) of 3-(2-chloro-pyrimidin-4-yl)-8-oxa-3-aza-bicyclo[3.2.1]octane (3) along with 50 mg (0.22 mmol, 4%) of 3-(4-chloro-pyrimidin-2-yl)-8-oxa-3-aza-bicyclo[3.2.1]octane (4).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835429B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-42bc12a8e8aa4652ad482317cfda17d5
출처 메모uspto-grants-2014_09