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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75457생성일: 2026년 10월 25일

Triethylamine → 8-(2-Chloro-6-(chloromethyl)pyrimidin-4-yl)-3-oxa-8-azabicyclo[3.2.1]octane

https://huagongshe.com/reaction/75457

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,4-Dichloro-6-(chloromethyl)pyrimidineHCID 15001778—
반응물3-Oxa-8-azabicyclo(3.2.1)octane hydrochlorideHCID 53401129—
용매DichloromethaneHCID 6344—
생성물8-(2-Chloro-6-(chloromethyl)pyrimidin-4-yl)-3-oxa-8-azabicyclo[3.2.1]octaneHCID 8666590769%

반응 단계

A flask was charged with 2,4-dichloro-6-(chloromethyl)pyrimidine (prepared as reported in Bioorg. Med. Chem., 2002, 10, 525), 2.40 g, 12.15 mmol) in dichloromethane (30 mL) to give a yellow solution. 3-Oxa-8-azabicyclo[3.2.1]octane, HCl (33, 1.818 g, 12.15 mmol) and triethylamine (3.56 ml, 25.5 mmol) in dichloromethane (30 mL) were added slowly over 10 minutes, and the resulting solution was allowed to stir at room temperature for 16 hours, then concentrated. The crude product was added to a silica gel column and eluted with 0-40% ethyl acetate in hexanes to provide 8-(2-chloro-6-(chloromethyl)pyrimidin-4-yl)-3-oxa-8-azabicyclo[3.2.1]octane (2.30 g, 69%) as an off-white solid. HRMS; [M+H]+ Obs'd=274.0510, [M+H]+ Calc'd=274.0508

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835429B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-10012ad628a540849ce16f926bf6d2d0
출처 메모uspto-grants-2014_09