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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1269927생성일: 2026년 10월 25일

Triphenylphosphine → HCID 22933948, 화합물

https://huagongshe.com/reaction/1269927

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물tert-Butyl 4-hydroxyazepane-1-carboxylateHCID 22933363—
반응물4-(methylthio)-1H-indazol-5-olHCID 22933648—
용매TetrahydrofuranHCID 8028—
생성물HCID 22933948HCID 2293394840%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07199147B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-42e7362441c44e01897ad1fd73e07ef0
출처 메모uspto-grants-2007_04