참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 6-Chloro-3-pyridinecarbonitrile | HCID 5152094 | — |
| 반응물 | 1-Isopropyl-4-(piperidine-4-carbonyl)-piperazine | HCID 28282195 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 799557-88-3 | HCID 68817996 | 39.9% |
반응 단계
To 1-isopropyl-4-(piperidine4-carbonyl)-piperazine (0.239 g)(D1) and 2-chloro-5-cyano-pyridine (0.138 g), dissolved in DMSO (5 ml), was added potassium carbonate (0.14 g). The reaction was heated to 80° C. for 4 h before cooling and dilution with saturated sodium hydrogen carbonate (50 ml) and EtOAc (80 ml). The EtOAc layer was washed further with brine (3×80 ml) and then extracted with 1N HCl. The aqueous HCl extract was basified and back-extracted with EtOAc which was concentrated under vacuum. A solution of 2N HCl in diethyl ether (1 ml) was then added and the precipitate filtered and washed with diethyl ether. Crystallisation from methanol afforded the title compound (E1)(0.15 g). 1H NMR δ [DMSO-d6]:1.29 (6H, d, J=6.4 Hz), 1.4-1.6 (2H, m), 1.7-1.85 (2H, m), 2.8-3.27 (6H, m), 3.32-3.62 (3H, m), 3.69 (1H, m), 4.24 (1H, brd, J=13 Hz), 4.35-4.55 (3H, m), 6.96 (1H, d, J=9.1 Hz), 7.84 (1H, dd, J=9.1Hz and 1.5 Hz), 8.47 (1H, d, J=1.5 Hz) and 11.36 (1H, brs). MS electrospray; (+ve ion) 342 (MH+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07592347B2 |
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| 출처 데이터셋 | uspto-grants-2009_09 |
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| ORD ID | ord-eef5cd896ae542688a5745cf2f88775e |
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| 출처 메모 | uspto-grants-2009_09 |
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