참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chloroacetaldehyde | HCID 33 | — |
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | 2,6-Diaminopyridine | HCID 8861 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 용매 | Sodium Chloride | HCID 5234 | — |
| 생성물 | Imidazo[1,2-a]pyridin-5-amine | HCID 327952 | 22% |
반응 단계
To a solution of 2,6-diaminopyridine (5.00 g, 45.8 mmol) in 1:1H2O:EtOH (10 mL) were added sodium bicarbonate (5.00 g, 59.5 mmol) and chloroacetaldehyde (4.31 g, 27.5 mmol). The reaction mixture was heated to 70° C. overnight, then cooled to rt, diluted with saturated aqueous NaCl (100 mL), and extracted with n-butanol (3×200 mL). The organic layers were combined, dried (MgSO4), and concentrated. The crude residue was purified (FCC, 2 N NH3 in MeOH/DCM) to give imidazo[1,2-a]pyridin-5-ylamine (1.32 g, 22%). MS (ESI+): calcd for C7H7N3 m/z 133.06, found 134.1 (M+H)+. 1H NMR (d6-DMSO): 8.23-8.21 (m, 1H), 7.91 (d, J=1.3, 1H), 7.50 (dd, J=8.8, 7.4, 1H), 7.22 (d, J=8.8, 1H), 6.97 (br s, 2H), 6.37 (dd, J=7.4, 0.9, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08877769B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-545dbf0f64434acab0928dfc9354bc3c |
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| 출처 메모 | uspto-grants-2014_11 |
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