Hydrochloric Acid → HCID 21073887、化合物
反応式
[C:1]1([N:11]2[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][CH2:19][CH:20]=[CH:21][C:22]3[N:31]=[C:30]4[C:25]([CH2:26][CH2:27][C:28](=[O:32])[NH:29]4)=[CH:24][CH:23]=3)[CH2:13][CH2:12]2)[C:10]2[CH2:9][CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.Cl>C1COCC1.CCOCC.[Ni]>[C:1]1([N:11]2[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][C:22]3[N:31]=[C:30]4[C:25]([CH2:26][CH2:27][C:28](=[O:32])[NH:29]4)=[CH:24][CH:23]=3)[CH2:13][CH2:12]2)[C:10]2[CH2:9][CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1参加物
6
実験手順
7-{5-[4-(5,6,7,8-Tetrahydro-naphthalen-1-yl)-piperazin-1-yl]-pent-1-enyl}-3,4-dihydro-1H-[1,8]naphthyridin-2-one (0.225 g, 0.523 mmol) was hydrogenated using Ra—Ni (0.25 g) in THF for 16 hours. The reaction was filtered and concentrated to give a foam. This was dissolved in Et2O and 1M HCl in Et2O (1 equiv) was added. The precipitate was filtered and dried to give the title compound as a white solid (0.157 g, 70%). MS: APCI: M+1: 433.4 (Exact Mass: 432.29).
後処理
- customfor 16 hours
- filtrationThe reaction was filtered
- concentrationconcentrated
- customto give a foam
- filtrationThe precipitate was filtered
- customdried
出典と根拠
- ORDレコード
- ord-3d445e8b459b4a78884dd49293bee55c
- 出典データセット
- uspto-grants-2007_01
- 特許番号
- US07160888B2
反応ノート
読み込み中…