Phenethylamine → HCID 89837825、化合物

HRID 1050738ノート

反応式

HRID 1050738 の反応式
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

6

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

  1. customirradiated with microwave 250 W
  2. temperatureto refluxing for 15 min
  3. washwashed with water (2×50 mL)
  4. additionThe ethyl acetated solution was mixed with water (50 mL)
  5. customkept at rt
  6. customto give solid form
  7. 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…