참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl 3-oxo-3-(pyridin-2-yl)propanoate | HCID 2736461 | — |
| 반응물 | HCID 178418690 | HCID 178418690 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | HCID 178422350 | HCID 178422350 | 79% |
반응 단계
(prepared according to an analogous procedure described in Polish J. Chem., 56 (1982) p 963) 3-Oxo-3-(pyridin-2-yl)propionic acid ethyl ester (2 g, 0.01035 mol) and 5-methyl-2H-pyrazol-3-ylamine (1 g, 1 eq) were heated together at 140° C. for 2 h; after cooling to rt, the solid residue was stirred with EtOAc and the solid collected by filtration to give 1.84 g of 2-methyl-5-pyridin-2-yl-4H-pyrazolo[1,5-a]pyrimidin-7-one. Step B: The product of step A (1.84 g) was dissolved in POCl3 (24 ml) and cooled to 0° C. N,N-dimethylaniline (3.1 ml, 3 eq) was added and the mixture heated at 60° C. for 16 h. The mixture was cooled to rt and the volatiles removed. The resulting residue was dissolved in CH2Cl2, poured onto ice, and taken to pH 8 with NaHCO3 (s). The CH2Cl2 layer was removed, washed with water, and dried (MgSO4). The mixture was concentrated under reduced pressure and the residue chromatographed (SiO2, hexane-EtOAc/hexane 1:1) to give 1.2 g of the title compound. 1H NMR (CDCl3) δ 8.71 (m, 1H), 8.49 (d, J=8.4 Hz, 1H), 8.14 (s, 1H), 7.87 (t, J=9.6 Hz, 1H), 7.41 (m, 1H), 6.64 (s, 1H), 2.60 (s, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07741318B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-fa552a407fcc4f58a45641c49b7bc2f8 |
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| 출처 메모 | uspto-grants-2010_06 |
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