反応式
[C:1]([O:5][C:6]([NH:8][C@H:9]([CH2:18][CH2:19][CH2:20][CH2:21][NH:22][C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])[C:10]([NH:12][CH2:13][CH2:14][C:15]([OH:17])=[O:16])=[O:11])=[O:7])([CH3:4])([CH3:3])[CH3:2].C1CCC(N=C=NC2CCCCC2)CC1.[CH3:45][C:46]([NH:48][CH:49]1[C:59]2[CH:60]=[C:61](O)[CH:62]=[CH:63][C:58]=2[C:57]2[C:52](=[CH:53][C:54]([O:69][CH3:70])=[C:55]([O:67][CH3:68])[C:56]=2[O:65][CH3:66])[CH2:51][CH2:50]1)=[O:47]>CN(C1C=CN=CC=1)C.ClCCl>[C:1]([O:5][C:6]([NH:8][C@H:9]([CH2:18][CH2:19][CH2:20][CH2:21][NH:22][C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])[C:10]([NH:12][CH2:13][CH2:14][C:15]([O:17][C:61]1[CH:62]=[CH:63][C:58]2[C:57]3[C:56]([O:65][CH3:66])=[C:55]([O:67][CH3:68])[C:54]([O:69][CH3:70])=[CH:53][C:52]=3[CH2:51][CH2:50][C@H:49]([NH:48][C:46](=[O:47])[CH3:45])[C:59]=2[CH:60]=1)=[O:16])=[O:11])=[O:7])([CH3:4])([CH3:3])[CH3:2]参加物
6
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
A mixture of 3-{[(2R)-2,6-di(tertbutoxycarbonylamino)hexanoyl]amino}propanoic acid (2) (0.178 g; 0.5 mmol), DCCI (0.124 g; 0.6 mmol), DMAP (0.013 g; 0.1 mmol) and N-acetyl-colchicinol (0.25 g; 1.2 mmol) in dichloromethane was stirred under argon atmosphere at ambient temperature for 5 hours. After filtration of the insoluble material the residue was purified by flash chromatography eluting with dichloromethane/ethanol (95/5) to give (1).
後処理
- filtrationAfter filtration of the insoluble material the residue
- customwas purified by flash chromatography
- washeluting with dichloromethane/ethanol (95/5)
出典と根拠
- ORDレコード
- ord-114634f21c3a4a9fa0eecc265ffb4bb8
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07135502B1
関連ノート
読み込み中…