N,N-Diethylaniline → 4-Chloroimidazo[1,2-a]quinoxaline
反応式
[CH:1]1[N:5]2[C:6]3[C:11]([NH:12][C:13](=O)[C:4]2=[N:3][CH:2]=1)=[CH:10][CH:9]=[CH:8][CH:7]=3.C(N(CC)C1C=CC=CC=1)C.C(Cl)[Cl:27].CO>P(Cl)(Cl)(Cl)=O>[Cl:27][C:13]1[C:4]2[N:5]([CH:1]=[CH:2][N:3]=2)[C:6]2[C:11]([N:12]=1)=[CH:10][CH:9]=[CH:8][CH:7]=2参加物
実験手順
Compound 11 (1.4 g, 6.4 mmol) is solubilized in phosphorus oxychloride (24 ml), and N,N-diethylaniline (3.6 ml). The reaction mixture obtained is carried to reflux for approximately 2 h. The product is insoluble in POCl3 even after heating. The reaction is monitored by TLC, eluent: CH2Cl2/MeOH (95/5). TLC shows the presence of the end product, but also the appearance of breakdown products. The reaction mixture is dark brown in colour. The POCl3 is evaporated under vacuum. The residue is cooled in an ice bath before adding a little water and, dropwise, a saturated sodium bicarbonate solution to neutralize POCl3. A light yellow foam and a brown precipitate appear. The solid is isolated by filtration and is recrystallized in methanol. A beige solid (0.97 g, 75%) is obtained; 1H NMR (300 MHz, DMSO-d6) δ: 8.5 (s, 1H, N—CH—C), 8.06 (d, 1H, ArH), 7.56 (s, 1H, C—CH—N), 7.35 (m, 1H, ArH), 7.25 (m, 2H, ArH). Analysis calculated for C10H6N3C1: C, 58.98; H, 2.97; N, 20.64. Experimental: C, 59.12; H, 2.76; N, 20.45.
後処理
- customThe reaction mixture obtained
- temperatureto reflux for approximately 2 h
- temperatureafter heating
- customThe POCl3 is evaporated under vacuum
- temperatureThe residue is cooled in an ice bath
- additionbefore adding a little water
- customThe solid is isolated by filtration
- customis recrystallized in methanol
出典と根拠
- ORDレコード
- ord-868b9243070e4501ab42b4d893cf4864
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08378098B2
反応ノート
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