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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72708생성일: 2026년 10월 23일

Azetidine → 4-(Azetidin-1-yl)-6-chloropyrimidine-5-carbaldehyde

https://huagongshe.com/ko/reaction/72708

반응식

참여 물질

역할이름HCID투입량
반응물AzetidineHCID 10422—
반응물4,6-Dichloro-5-pyrimidinecarbaldehydeHCID 819691—
촉매TriethylamineHCID 8471—
용매ChloroformHCID 6212—
생성물4-(Azetidin-1-yl)-6-chloropyrimidine-5-carbaldehydeHCID 86712562—

반응 단계

To a solution of 4,6-dichloropyrimidine-5-carbaldehyde (1.00 g, 5.65 mmol) in chloroform at 0° C. were added azetidine (99%, 0.392 mL, 5.71 mmol) and triethylamine (5 drops). The reaction mixture was allowed to warm to room temperature and then stirred for 18 hours. The reaction mixture was filtered, and the filtrate was purified by silica gel chromatography (Gradient: 0% to 100% ethyl acetate in heptane) to provide the product. Yield: 880 mg, 4.45 mmol, 79%. LCMS m/z 198.1, 200.1 (M+1). 1H NMR (400 MHz, CD3OD) δ 2.34-2.43 (m, 2H), 4.12-4.33 (br m, 4H), 8.30 (s, 1H), 10.28 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829010B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-50b2e28456f84a5494615235ad31a5bc
출처 메모uspto-grants-2014_09