Phosphorus oxychloride → HCID 178515262, 화합물
반응식
O[C:2]1[N:3]([C:12]2[CH:13]=[N:14][C:15]([Cl:18])=[CH:16][CH:17]=2)[C:4](=[O:11])[C:5]2[N:6]=[CH:7][NH:8][C:9]=2[N:10]=1.P(Cl)(Cl)([Cl:21])=O>>[Cl:21][C:2]1[N:3]([C:12]2[CH:13]=[N:14][C:15]([Cl:18])=[CH:16][CH:17]=2)[C:4](=[O:11])[C:5]2[N:6]=[CH:7][NH:8][C:9]=2[N:10]=1참가 물질
반응 조건
- 온도
- 135 °C
실험 절차
2-Hydroxy-1-(6-chloropyridin-3-yl)-1,9-dihydro-6H-purin-6-one from the above reaction is suspended in a large excess of phosphorous oxychloride (150 mL) and heated to 135° C. for 24 h. The reaction mixture is cooled, evaporated in vacuo, and additional toluene is added and evaporated (2×) under reduced pressure. The resulting sticky brown oil is dissolved in DCM (200 mL), and then neutralized with saturated NaHCO3 (aqueous). The aqueous layer is extracted with DCM (2×200 mL) and dried (MgSO4). The dried extract is filtered and concentrated under vacuum to afford crude product as a light brown solid. The crude product is purified by flash column chromatography using 1-2.5% MeOH/CH2Cl2 to afford the title compound as white solid. 1H NMR (300 MHz, CDCl3) δ 8.33 (s, 1H), 7.78 (s, 1H), 7.58 (d, J=6 Hz, 1H), 7.53 (d, J=6 Hz, 1H).
후처리
- temperatureThe reaction mixture is cooled
- customevaporated in vacuo, and additional toluene
- additionis added
- customevaporated (2×) under reduced pressure
- dissolutionThe resulting sticky brown oil is dissolved in DCM (200 mL)
- extractionThe aqueous layer is extracted with DCM (2×200 mL)
- dry with materialdried (MgSO4)
- extractionThe dried extract
- filtrationis filtered
- concentrationconcentrated under vacuum
- customto afford crude product as a light brown solid
- customThe crude product is purified by flash column chromatography
출처 및 근거
- ORD 기록
- ord-2426e61268434530a16ef08820220c0b
- 출처 데이터셋
- uspto-grants-2014_06
- 특허 번호
- US08759361B2
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