Sodium Hydroxide → methyl (R)-2-(3-1H-imidazol-4-ylpropionylamino)-3-(4-methoxyphenyl)propanoate
反応式
CCN(C(C)C)C(C)C.Cl.[CH2:11]([C:18]([OH:20])=O)[CH2:12][C:13]1[N:17]=[CH:16][NH:15][CH:14]=1.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.[NH2:43][C@H:44]([CH2:49][C:50]1[CH:55]=[CH:54][C:53]([O:56][CH3:57])=[CH:52][CH:51]=1)[C:45]([O:47][CH3:48])=[O:46].[OH-].[Na+]>CN(C=O)C>[NH:15]1[CH:14]=[C:13]([CH2:12][CH2:11][C:18]([NH:43][C@H:44]([CH2:49][C:50]2[CH:51]=[CH:52][C:53]([O:56][CH3:57])=[CH:54][CH:55]=2)[C:45]([O:47][CH3:48])=[O:46])=[O:20])[N:17]=[CH:16]1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 1
実験手順
35.5 ml of DIEA are added to a solution containing 13.2 g (74.7 mmol) of desamino-histidine hydrochloride and 24 g (74.7 mmol) of TBTU in 100 ml of DMF. After stirring for 15 minutes at ambient temperature, 14.2 g (67.9 mmol) of methyl (R)-2-amino-3-(4-methoxyphenyl)-propanoate in 150 ml of DMF are added. The reaction medium is left to stir for 16 hours and then basified to pH=8-9 by introducing 1N sodium hydroxide and a saturated solution of sodium hydrogen carbonate, followed by extraction with dichloromethane. The organic phase is dried over sodium sulphate, filtered and evaporated. The crude product obtained is purified by silica gel chromatography (eluent 85/15 dichloromethane/methanol). 11.0 g in the form of an orange oil are obtained with a yield of 49%.
後処理
- waitThe reaction medium is left
- stirringto stir for 16 hours
- extractiona saturated solution of sodium hydrogen carbonate, followed by extraction with dichloromethane
- dry with materialThe organic phase is dried over sodium sulphate
- filtrationfiltered
- customevaporated
出典と根拠
- ORDレコード
- ord-cad5a82c6e154366b59be598db2208ee
- 出典データセット
- uspto-grants-2014_10
- 特許番号
- US08871187B2
反応ノート
読み込み中…