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HRID 1269927作成日:2026年10月27日

Triphenylphosphine → tert-butyl 4-{[4-(methylthio)-1H-indazol-5-yl]oxy}azepane-1-carboxylate

https://huagongshe.com/reaction/1269927

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 diazene-1,2-dicarboxylateHCID 75555—
反応物tert-Butyl 4-hydroxyazepane-1-carboxylateHCID 22933363—
反応物4-(methylthio)-1H-indazol-5-olHCID 22933648—
溶媒TetrahydrofuranHCID 8028—
生成物tert-butyl 4-{[4-(methylthio)-1H-indazol-5-yl]oxy}azepane-1-carboxylateHCID 2293394840%

反応手順

The tert-butyl 4-hydroxyazepane-1-carboxylate (0.0504 g, 0.23 mmol) obtained in Example 322, (c) and triphenylphosphine (0.0723 g, 0.28 mmol) were added to a solution of the 4-(methylthio)-1H-indazol-5-ol (0.0377 g, 0.21 mmol) obtained in Example 607 in tetrahydrofuran (2 ml), and the resulting mixture was ice-cooled. A solution of diisopropyl azodicarboxylate (0.0557 g, 0.28 mmol) in tetrahydrofuran (1 ml) was added dropwise thereto, and the resulting mixture was slowly heated to room temperature and stirred overnight. The reaction solution was concentrated and then diluted with chloroform, and a 1N-aqueous sodium hydroxide solution was added thereto, followed by extraction with chloroform (twice). The extract solution was dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by a silica gel chromatography (hexane/ethyl acetate=3/1˜2/1˜3/2) to obtain tert-butyl 4-{[4-(methylthio)-1H-indazol-5-yl]oxy}azepane-1-carboxylate (0.0318 g, 40%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07199147B2
出典データセットuspto-grants-2007_04
ORD IDord-42e7362441c44e01897ad1fd73e07ef0
出典メモuspto-grants-2007_04