4-Amino-1-(2-naphthyl)methylpiperidine → Hydrochloric Acid
反応式
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[CH:10]=2)[C:5]([CH2:14][O:15][CH3:16])=[N:4][N:3]=1.[NH2:17][CH:18]1[CH2:23][CH2:22][N:21]([CH2:24][C:25]2[CH:34]=[CH:33][C:32]3[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=3)[CH:26]=2)[CH2:20][CH2:19]1>C(O)(C)C>[ClH:1].[CH3:13][O:12][C:9]1[CH:10]=[C:11]2[C:6]([C:5]([CH2:14][O:15][CH3:16])=[N:4][N:3]=[C:2]2[NH:17][CH:18]2[CH2:19][CH2:20][N:21]([CH2:24][C:25]3[CH:34]=[CH:33][C:32]4[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=4)[CH:26]=3)[CH2:22][CH2:23]2)=[CH:7][CH:8]=1.[ClH:1]参加物
5
実験手順
This compound is obtained according to the procedure described in 1.4. by reacting 1-chloro-7-methoxy-4-methoxymethylphthalazine with 4-amino-1-(naphthalen-2-ylmethyl)piperidine. The hydrochloride is obtained after treatment with a solution of hydrogen chloride in isopropanol.
後処理
- customThis compound is obtained
出典と根拠
- ORDレコード
- ord-c085fe0b9ecf443f9a13075454922195
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07423030B2
反応ノート
読み込み中…