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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1875926생성일: 2026년 10월 27일

Cesium carbonate → (R)-N-(6-phenoxypyrimidin-4-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine

https://huagongshe.com/reaction/1875926

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물DiisopropylcarbodiimideHCID 12734—
반응물4-Isothiocyanato-6-phenoxypyrimidineHCID 57476567—
반응물(S)-3-(aminomethyl)quinuclidin-3-ol dihydrochlorideHCID 66724709—
용매DimethylformamideHCID 6228—
생성물(R)-N-(6-phenoxypyrimidin-4-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amineHCID 5808817297%

반응 단계

To (S)-3-(aminomethyl)quinuclidin-3-ol dihydrochloride (0.170 g, 0.742 mmol) in N,N-dimethylformamide (20 mL) was added Cs2CO3 (0.604 g, 1.854 mmol) and 4-isothiocyanato-6-phenoxypyrimidine (0.17 g, 0.742 mmol). The suspension was stirred at room temperature for 30 minutes. N,N′-diisopropylcarbodiimide (0.347 mL, 2.225 mmol) was then added and the mixture was continued to stir at room temperature for 18 hours. The mixture was concentrated and purified by silica gel chromatography (5-25% 9:1 methanol:ammonium hydroxide-ethyl acetate) to afford (R)—N-(6-phenoxypyrimidin-4-yl)-4H-1′-azaspiro[oxazole-5,3′-bicyclo[2.2.2]octan]-2-amine (0.21 g, 0.72 mmol, 48.2% yield) as a pale yellow solid. 1H NMR (500 MHz, MeOD) δ ppm 8.43 (1H, s), 7.47 (2H, t), 7.30 (1H, t), 7.16 (2H, d), 6.21 (1H, br. s.), 4.03 (1H, d), 3.72 (1H, d), 3.22 (1H, d), 3.11 (1H, d), 2.73-2.99 (4H, m), 2.00-2.18 (2H, m), 1.54-1.88 (3H, m). LCMS R.T.=1.46; [M+H]+=352.19.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309577B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-24109fdf3bbd40a2b27a7939ce63a46c
출처 메모uspto-grants-2012_11