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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 875942생성일: 2026년 10월 23일

Ethyl Acetate → 5-Bromo-2-chloro-N-(tetrahydro-2H-pyran-4-yl)pyrimidin-4-amine

https://huagongshe.com/ko/reaction/875942

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물DiisopropylethylamineHCID 81531—
반응물5-Bromo-2,4-dichloropyrimidineHCID 289973—
반응물4-AminotetrahydropyranHCID 419223—
용매1,4-DioxaneHCID 31275—
생성물5-Bromo-2-chloro-N-(tetrahydro-2H-pyran-4-yl)pyrimidin-4-amineHCID 59550890105.4%

반응 단계

5-Bromo-2,4-dichloropyrimidine (5.0 g, 21.9 mmol), tetrahydro-2H-pyran-4-amine (2.22 g, 21.9 mmol), and N-ethyl-N-isopropylpropan-2-amine (4.25 g, 32.9 mmol) were dissolved in dioxane (50 ml) and the reaction was stirred at room temperature for 12 hours. Ethyl acetate was added to the reaction mixture and the organic layer was washed with water and brine. The organic layer was dried with sodium sulfate. Removal of solvent gave (5-bromo-2-chloro-pyrimidin-4-yl)-(tetrahydro-pyran-4-yl)-amine (32) as a light yellow solid (6.75 g, 99%). 1H NMR (500 MHz, CD3OD) δ ppm 8.04 (1 H, s), 4.14-4.21 (1 H, m), 3.89 (2 H, dd, J=11.4, 4.3 Hz) 3.43 (2 H, td, J=11.9, 2.0 Hz), 1.80 (2 H, ddd, J=12.6, 4.2, 1.8 Hz), 1.63 (2 H, qd, J=12.2, 4.5, Hz); LCMS-ESI (POS), M/Z, M+1: Found 292.0, Calculated 292.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08980903B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-85091248ae344965ba2f9333eb73f4d4
출처 메모uspto-grants-2015_03