HCID 22891997、化合物 → HCID 69940044、化合物
反応式
[CH2:1]([O:8]C([N:11]1[CH2:16][CH2:15][CH:14]([CH2:17][N:18]2[C:22]([CH2:23][N:24]3[CH:28]=[C:27]([C:29]([N:31]4[CH2:36][CH2:35][O:34][CH2:33][CH2:32]4)=[O:30])[C:26]([C:37]4[C:46]5[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=5)[CH:40]=[CH:39][CH:38]=4)=[N:25]3)=[CH:21][N:20]=[CH:19]2)[CH2:13][CH2:12]1)=O)C1C=CC=CC=1.[H][H]>CO.[C+4].[OH-].[Pd+2].[OH-].[OH-].[OH-].[OH-].[OH-]>[OH2:8].[NH3:11].[CH3:1][OH:8].[NH:11]1[CH2:12][CH2:13][CH:14]([CH2:17][N:18]2[C:22]([CH2:23][N:24]3[CH:28]=[C:27]([C:29]([N:31]4[CH2:36][CH2:35][O:34][CH2:33][CH2:32]4)=[O:30])[C:26]([C:37]4[C:46]5[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=5)[CH:40]=[CH:39][CH:38]=4)=[N:25]3)=[CH:21][N:20]=[CH:19]2)[CH2:15][CH2:16]1参加物
6
実験手順
227 mg (0.36 mmol) of the compound prepared in Example 158 was dissolved in methanol, 20 mg of palladium hydroxide carbon was added thereto, and the mixture was reacted under 1 atm of hydrogen for 2 hours. After the reaction was completed, the mixture was filtered and the solvent therein was removed. The residue was subjected to silica gel column chromatography(eluent: ammonia water/methanol=15/85, v/v) to give 120 mg (0.26 mmol, Yield 74%) of the title compound.
後処理
- filtrationthe mixture was filtered
- customthe solvent therein was removed
出典と根拠
- ORDレコード
- ord-609d34d020a544c09ff8a043d3d4ad85
- 出典データセット
- uspto-grants-2002_10
- 特許番号
- US06472526B1
反応ノート
読み込み中…