참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,4-Dichloropyrimidine | HCID 77531 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | HCID 178507266 | HCID 178507266 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | HCID 178478345 | HCID 178478345 | 81% |
반응 단계
A dried 5-L, three-neck round bottom flask fitted with an overhead stirrer and reflux condenser was charged with a solution of 2,4-dichloropyrimidine (250 g, 1.678 mol) in anhydrous DMSO (2300 mL). 3-Cyclopropyl-1H-pyrazol-5-amine (227.4 g, 1.8458 mol) and DIPEA (438 mL, 2.517 mol) were added sequentially at RT. The resulting solution was stirred at 60° C. for 16 h, cooled to RT, and poured into ice water. The precipitated yellow solid was collected by vacuum filtration, and washed well with water, 1.5 N HCl (3×1 L), and finally rinsed of water (4×500 mL). The precipitate was dried by air suction overnight to give 320 g (81%) of 53 as yellow solid: 1H NMR (400 MHz, DMSO-d6) δ 12.19 (s, 1H), 10.29 (s, 1H), 8.15 (s, 1H), 7.0 (br s, 1H), 6.0 (br s, 1H), 1.85-1.92 (m, 1H), 0.91-0.95 (m, 2H), 0.7 (m, 2H); MS (ESI+) m/z=236 [M+1]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08637537B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-11c670b1fb46476694d509ac35afb37c |
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| 출처 메모 | uspto-grants-2014_01 |
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