反応式
Cl.[NH:2]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH:12]=[CH:13][C:14]([NH2:16])=[O:15])[C:3]([NH2:5])=[NH:4].Cl.Cl.[NH2:19][CH2:20][CH2:21][CH2:22][NH:23][CH2:24][CH2:25][CH2:26][CH2:27][NH:28][C:29](=[O:33])[CH:30](O)[OH:31].C(O)(=O)CCCC(O)=O.Cl.Cl.Cl.N(CCCCCCC=CC(NC(O)C(N)=O)=O)C(N)=N>O>[NH2:19][CH2:20][CH2:21][CH2:22][NH:23][CH2:24][CH2:25][CH2:26][CH2:27][NH:28][C:29](=[O:33])[CH:30]([NH:16][C:14](=[O:15])[CH:13]=[CH:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][NH:2][C:3]([NH2:5])=[NH:4])[OH:31]参加物
6
反応条件
- 温度
- 60 °C
実験手順
A mixture of 206.2 mg (0.84 mmole) of 9-guanidino-2-nonenamide hydrochloride, 291.0 mg (1.00 mmole) of N-[4-(3-aminopropyl)aminobutyl]-2,2-dihydroxyethanamide dihydrochloride, 109.6 mg (0.84 mmole) of glutaric acid and 0.2 ml of water was heated at 60° C. for 24 hours. After completion of the reaction, the reaction mixture was purified in a manner similar to that in Example 1 using CM-Sephadex® C-25 (Na-type) and Sephadex® LH-20 to obtain 135.0 mg (31.1% yield) of a white powder of N-[4-(3-aminopropyl)aminobutyl]-2-(9-guanidino-2-nonenamido-2-hydroxyethanamide trihydrochloride.
後処理
- customAfter completion of the reaction
- customthe reaction mixture was purified in a manner similar to that in Example 1 using CM-Sephadex®
出典と根拠
- ORDレコード
- ord-dc615805a55a42cf8a30f6d2f2018da6
- 出典データセット
- uspto-grants-1985_05
- 特許番号
- US04518532
関連ノート
読み込み中…