8-Amino-1,4-diethyl-1,2,3,4-tetrahydro-benzo[e][1,4]diazepin-5-one → 1,4-Diethyl-2,3,4,5-tetrahydro-1H-1,4-benzodiazepin-8-ylamine
反応式
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]2[C:11](=O)[N:10]([CH2:13][CH3:14])[CH2:9][CH2:8][N:7]([CH2:15][CH3:16])[C:6]=2[CH:17]=1>O1CCOCC1.C1COCC1>[CH2:15]([N:7]1[C:6]2[CH:17]=[C:2]([NH2:1])[CH:3]=[CH:4][C:5]=2[CH2:11][N:10]([CH2:13][CH3:14])[CH2:9][CH2:8]1)[CH3:16]参加物
反応条件
- 温度
- 75 °C
実験手順
To a solution of 8-Amino-1,4-diethyl-1,2,3,4-tetrahydro-benzo[e][1,4]diazepin-5one (22.0 g, 0.0944 mol) in dioxane (400 mL) was added borane dimethyl sulfide complex solution (2 M in THF, 118 mL, 0.236 mol) and heated at 75° C. for 4 hr. The reaction was quenched with ethanol (100 mL) and stirred at room temperature for 18 hr., then evaporated. To the residue was added hydrazine hydrate (100 mL) and heated at 95° C. for 4 hr. After evaporation, toluene (50 mL) and ethanol (50 mL) werer added, distilled and the reaction evaporated. The residue was extracted with DCM, evaporated, dissolved in ether, filtered and evaporated to give 1,4-Diethyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepin-8-ylamine as an oil (16.0 g, 84%). LCMS (m/e) 220 (M+1); 1H-NMR (DMSO, 400 MHz) δ 6.79-6.71 (d, 1H, J=7.83 Hz), 6.49 (br, 1H,), 6.01-5.99 (d, 1H, J=7.83 Hz), 4.79 (s, 2H), 3.07-3.02 (q, 2H, J=6.82 Hz), 2.85-2.83 (t, 2H, J=8.08 Hz), 2.70-2.68 (t, 2H, J=8.09 Hz), 1.13-1.10 (t, 3H, J=7.07 Hz), 1.00-0.97 (t, 3H, J=7.32 Hz),
後処理
- customThe reaction was quenched with ethanol (100 mL)
- custom, then evaporated
- additionTo the residue was added hydrazine hydrate (100 mL)
- temperatureheated at 95° C. for 4 hr
- customAfter evaporation, toluene (50 mL) and ethanol (50 mL) werer
- additionadded
- distillationdistilled
- customthe reaction evaporated
- extractionThe residue was extracted with DCM
- customevaporated
- dissolutiondissolved in ether
- filtrationfiltered
- customevaporated
出典と根拠
- ORDレコード
- ord-f9ab161f2e164853997731f9b65bde4e
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08552186B2
反応ノート
読み込み中…