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HRID 571728作成日:2026年10月27日

(2-benzyloxy-7,8-dihydro-4H,6H-1,5,8a-triaza-azulen-5-yl)-(4-fluoro-phenyl)-methanone → HCID 178519626、化合物

https://huagongshe.com/reaction/571728

反応式

関与物質

役割名称HCID仕込み量
反応物(2-benzyloxy-7,8-dihydro-4H,6H-1,5,8a-triaza-azulen-5-yl)-(4-fluoro-phenyl)-methanoneHCID 86706495—
触媒Palladium hydroxideHCID 9942167—
溶媒N,N-dimethylformamide ethyl acetateHCID 22989253—
生成物HCID 178519626HCID 17851962693%

反応手順

A solution of (2-benzyloxy-7,8-dihydro-4H,6H-1,5,8a-triaza-azulen-5-yl)-(4-fluoro-phenyl)-methanone (0.902 g, 2.47 mmol) in a mixture of AcOEt/DMF (25/25 mL) was hydrogenated in a H-Cube reactor (1.5 ml/min, 70 mm, Pd(OH)2/C cartridge, full H2 mode, 80° C., 1 cycle). The solvents were evaporated in vacuo to yield (4-Fluoro-phenyl)-(2-hydroxy-7,8-dihydro-4H,6H-1,5,8a-triaza-azulen-5-yl)-methanone (0.63 g, 93% yield) as a colorless oil, that was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09029366B2
出典データセットuspto-grants-2015_05
ORD IDord-814ca853f9ba4a78a4b73d309bc5f3b8
出典メモuspto-grants-2015_05