Phosphorus oxychloride → HCID 21113078、化合物
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:17]([C:18]2[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][CH:19]=2)[C:11]2[CH:12]=[N:13][NH:14][C:15](=O)[C:10]=2[N:9]=1.O=P(Cl)(Cl)[Cl:27]>>[Cl:27][C:15]1[N:14]=[N:13][CH:12]=[C:11]2[N:17]([C:18]3[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][CH:19]=3)[C:8]([C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=3[Cl:1])=[N:9][C:10]=12参加物
実験手順
A solution of 2-(2-chloro-phenyl)-1-(4-chloro-phenyl)-1,5-dihydro-imidazo[4,5-d]pyridazin-4-one (I-2g, 22 mg, 0.062 mmol) in POCl3 (3 ml) was heated under reflux for 2.5 hours. The reaction mixture was cooled to room temperature and the solvent was removed under vacuum. The residue was dissolved in toluene and again concentrated. This procedure was repeated twice. The residue was then taken up in CH2Cl2, and H2O was added. The pH of the aqueous solution was adjusted via addition of sat'd aq NaHCO3 until the pH was neutral (˜7). The CH2Cl2 layer was separated and the aqueous solution was extracted with CH2Cl2 (3×). The combined organic extracts were dried (Na2SO4) and concentrated in vacuo to give I-2h as a pale yellow oil (22 mg): +APCI MS (M+1) 375.0/377.0; 1H NMR (CDCl3) δ 7.18–7.23 (2H, m), 7.35–7.48 (5H, m), 7.56–7.60 (1H, m), 9.22 (1H, s).
後処理
- temperatureunder reflux for 2.5 hours
- customthe solvent was removed under vacuum
- dissolutionThe residue was dissolved in toluene
- concentrationagain concentrated
- additionH2O was added
- additionThe pH of the aqueous solution was adjusted via addition of sat'd aq NaHCO3 until the pH
- customThe CH2Cl2 layer was separated
- extractionthe aqueous solution was extracted with CH2Cl2 (3×)
- dry with materialThe combined organic extracts were dried (Na2SO4)
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-faf074460fe646579988711135c9cd32
- 出典データセット
- uspto-grants-2007_06
- 特許番号
- US07232823B2
反応ノート
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