참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | Ethyl imidazo[1,2-a]pyridine-6-carboxylate | HCID 11830209 | — |
| 반응물 | 5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamide | HCID 22449352 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1-cyclopentyl-3-ethyl-6-imidazo[1,2-a]pyridin-6-yl-2H-pyrazolo[3,4-d]pyrimidin-4-one | HCID 178437834 | 62% |
반응 단계
Sodium metal (0.21 g, 9.2 mmol) was dissolved in ethanol (25 ml) and 6-carboethoxyimidazo[1,2-a]pyridine (1.75 g, 9.2 mmol) and 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (1.02 g, 4.6 mmol) were added. The reaction mixture was heated to reflux for 24 hours, cooled to room temperature and stirred for 60 hours. The solvent was removed in vacuo, the residue was dissolved in water (100 ml) and the solution was neutralized by the addition of concentrated HCl. A precipitate was obtained which was collected by filtration through a glass frit. The solid was recrystallized from ethanol and washed with ether to afford 0.98 g (62%) of 1-cyclopentyl-3-ethyl-6-(6-imidazo[1,2-a]pyridinyl)-pyrazolo[3,4-d]pyrimidin-4-one as white crystals, m.p. >300° C. when dried for 18 hours at 120° C. in high vacuum.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05294612 |
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| 출처 데이터셋 | uspto-grants-1994_03 |
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| ORD ID | ord-19b4b463815840d1850298edd2de8c12 |
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| 출처 메모 | uspto-grants-1994_03 |
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