反応式
Br[CH2:2][C:3]([CH2:5]Br)=[O:4].[C:7]1([P:13]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)(=[O:15])[OH:14])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>[F-].[K+].CN(C=O)C>[C:7]1([P:13]([O:14][CH2:2][C:3]([CH2:5][O:15][P:13]([C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=2)([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[O:14])=[O:4])([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[O:15])[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1参加物
4
実験手順
(2S)-4-(tert-butoxy)-2-({[(5R)-5-isopropyl-3-(1-isoquinolinyl)-4,5-dihydro-5-isoxazolyl]carbonyl}amino)-4-oxobutanoic acid [obtained by coupling reaction of Compound (VIIf) with Asp(O-t-Bu)-OMe and hydrolysis] was reacted according to the same procedure as Preparation 5 to give bromomethyl ketone derivative (tert-butyl (3S)-5-bromo-3-({[(5R)-5-isopropyl-3-(1-isoquinolinyl)-4,5-dihydro-5-isoxazolyl]carbonyl}amino)-4-oxopentanoate). This bromomethyl ketone derivative was reacted with diphenylphosphinic acid in KF/DMF (see Preparation 5) to give diphenylphosphoryloxymethyl ketone derivative, which was then reacted according to the same procedure as Example 2 to give the title compound (Compound of Example 60).
出典と根拠
- ORDレコード
- ord-e8bf8f587d1544ea9954eb65e2e1a832
- 出典データセット
- uspto-grants-2009_07
- 特許番号
- US07557133B2
関連ノート
読み込み中…