Phenethylamine → HCID 89837825、化合物
反応式
CC(C(N)=O)[C:3]1[C:8]([C:9]([OH:11])=O)=[CH:7][C:6]([F:12])=[C:5]([Cl:13])[CH:4]=1.P(OC1C=CC=CC=1)(OC1C=CC=CC=1)OC1C=CC=CC=1.[CH2:39]([NH2:47])[CH2:40][C:41]1[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=1.[N:48]1C=C[CH:51]=[CH:50][CH:49]=1>C(OCC)(=O)C>[Cl:13][C:5]1[CH:4]=[C:3]2[C:8]([C:9](=[O:11])[N:47]([CH2:39][CH2:40][C:41]3[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=3)[C:49]([CH2:50][CH3:51])=[N:48]2)=[CH:7][C:6]=1[F:12]参加物
実験手順
The crude solid (3 g) from step 3 above mixed with triphenyl phosphite (4 mL, 14.81 mmol) in pyridine (15 mL) was stirred at rt for 4 h. The mixture was added with phenethylamine (1.55 mL, 12.18 mmol), irradiated with microwave 250 W to refluxing for 15 min. The mixture was diluted with ethyl acetate (50 mL), washed with water (2×50 mL). The ethyl acetated solution was mixed with water (50 mL) and kept at rt to give solid form. The solution was filtered to give yellow solid title compound (1.1 g, 27.2%). mp=150-152° C. (recrystallized from ethyl acetate); 1H NMR (400 MHz, DMSO-d6) δ 1.19 (t, J=7.2 Hz, 3H, CH3), 2.76 (q, J=7.2 Hz, 2H, CH2), 2.93 (br t, J=7.6 Hz, 2H, CH2), 4.19 (br t, J=7.6 Hz, 2H, CH2), 7.20-7.31 (m, 5H, ArH), 7.80 (d, J=6.4 Hz, 1H, ArH), 7.91 (d, J=8.8 Hz, 1H, ArH), 13C NMR (100 MHz, DMSO-d6) δ 10.6, 26.9, 33.5, 44.8, 112.2, 112.4, 119.8, 119.9, 126.6, 126.8, 127.0, 128.5, 128.7, 128.8, 138.0, 144.1, 153.6, 156.1, 158.9, 160.0; Anal. (C18H16ClFN2O) C, H, N. Calcd: 65.36, 4.88, 8.47. Found: 65.09, 4.77, 8.50.
後処理
- customirradiated with microwave 250 W
- temperatureto refluxing for 15 min
- washwashed with water (2×50 mL)
- additionThe ethyl acetated solution was mixed with water (50 mL)
- customkept at rt
- customto give solid form
- filtrationThe solution was filtered
出典と根拠
- ORDレコード
- ord-2ea9c1c789f047f29e2af3a2455dd4da
- 出典データセット
- uspto-grants-2016_07
- 特許番号
- US09387209B2
反応ノート
読み込み中…