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HRID 225953作成日:2026年10月27日

Diphenylphosphinic acid → Diphenylphosphoryloxymethyl ketone

https://huagongshe.com/reaction/225953

反応式

関与物質

役割名称HCID仕込み量
反応物Diphenylphosphinic acidHCID 15567—
反応物1,3-Dibromo-2-propanoneHCID 69952—
溶媒KF DmfHCID 86608353—
生成物Diphenylphosphoryloxymethyl ketoneHCID 54568997—

反応手順

(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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557133B2
出典データセットuspto-grants-2009_07
ORD IDord-e8bf8f587d1544ea9954eb65e2e1a832
出典メモuspto-grants-2009_07