反応式
[C:1]1([CH2:7][C:8]([NH:10][NH2:11])=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CO[C:14]1[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][N:21]=1>C1(C)C=CC=CC=1>[CH2:7]([C:8]1[N:21]2[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][C:14]2=[N:11][N:10]=1)[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
4
反応条件
- 温度
- 60 °C
実験手順
2-Phenylacetohydrazide (1.01 g) was added to a solution of anhydrous toluene (11 mL) and 8-methoxy-2,3,4,5,6,7-hexahydroazocine (0.96 mL). The mixture was warmed to 60° C. for 3 hours and heated to 110° C. overnight. The solution was cooled to room temperature and concentrated. The residue was purified by silica gel chromatography to give 3-benzyl-5,6,7,8,9,10-hexahydro[1,2,4]triazolo[4,3-a]azocine as a white solid.
後処理
- temperatureheated to 110° C. overnight
- temperatureThe solution was cooled to room temperature
- concentrationconcentrated
- customThe residue was purified by silica gel chromatography
出典と根拠
- ORDレコード
- ord-d465c185eb024b43b7e4a51e8c127967
- 出典データセット
- uspto-grants-2007_02
- 特許番号
- US07179802B2
関連ノート
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