Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 250060생성일: 2026년 10월 24일
Cesium carbonate → (R)-N-(6-phenoxypyrimidin-4-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine
https://huagongshe.com/ko/reaction/250060
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | Diisopropylcarbodiimide | HCID 12734 | — |
| 반응물 | 4-Isothiocyanato-6-phenoxypyrimidine | HCID 57476567 | — |
| 반응물 | (S)-3-(aminomethyl)quinuclidin-3-ol dihydrochloride | HCID 66724709 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (R)-N-(6-phenoxypyrimidin-4-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine | HCID 58088172 | 97% |
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 (1 H, s), 7.47 (2 H, t), 7.30 (1 H, t), 7.16 (2 H, d), 6.21 (1 H, br. s.), 4.03 (1 H, d), 3.72 (1 H, d), 3.22 (1 H, d), 3.11 (1 H, d), 2.73-2.99 (4 H, m), 2.00-2.18 (2 H, m), 1.54-1.88 (3 H, m). LCMS R.T.=1.46; [M+H]+=352.19.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07863291B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-f4390104ac6343748b55411ee6a8823e |
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| 출처 메모 | uspto-grants-2011_01 |
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