戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 331314作成日:2026年10月26日

Triphenylphosphine → tert-butyl 4-(3-(3-(3,5-difluorophenyl)-1-oxo-2-(pyridin-3-yl)-1H-inden-6-yloxy)propyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/331314

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diisopropyl azodicarboxylateHCID 5363146—
反応物1-Boc-4-(3-hydroxypropyl)piperazineHCID 16217800—
反応物2-bromo-6-hydroxy-3-phenyl-1H-inden-1-oneHCID 70306176—
反応物3-(3,5-difluorophenyl)-6-hydroxy-2-(pyridin-3-yl)-1H-inden-1-oneHCID 70317432—
生成物tert-butyl 4-(3-(3-(3,5-difluorophenyl)-1-oxo-2-(pyridin-3-yl)-1H-inden-6-yloxy)propyl)piperazine-1-carboxylateHCID 5100194085%

反応手順

The procedure of Step 6 of Example 1 was repeated except for using 3-(3,5-difluorophenyl)-6-hydroxy-2-(pyridin-3-yl)-1H-inden-1-one obtained in Step 1 as a starting material instead of 2-bromo-6-hydroxy-3-phenyl-1H-inden-1-one, t-butyl 4-(3-hydroxypropyl)piperazine-1-carboxylate (2.0 eq) instead of 4-(2-hydroxyethyl)morpholine, using 2 equivalents of PPh3 and DIAD, and being stirred for 19 h to obtain the title compound (85%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08877747B2
出典データセットuspto-grants-2014_11
ORD IDord-6eb869b9134e49538db3bc4426d2820c
出典メモuspto-grants-2014_11