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HRID 2199812作成日:2026年10月24日

(E)-6-methoxy-5-morpholino-2-(4-(trifluoromethyl)benzylidene)-2,3-dihydro-1H-inden-1-one → 6-methoxy-5-morpholino-2-(4-(trifluoromethyl) benzyl)-2, 3-dihydro-1H-inden-1-one

https://huagongshe.com/ja/reaction/2199812

反応式

関与物質

役割名称HCID仕込み量
反応物(E)-6-methoxy-5-morpholino-2-(4-(trifluoromethyl)benzylidene)-2,3-dihydro-1H-inden-1-oneHCID 117940206—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物6-methoxy-5-morpholino-2-(4-(trifluoromethyl) benzyl)-2, 3-dihydro-1H-inden-1-oneHCID 117940116—

反応手順

The 85 (50 mg, 0.123 mmol) was dissolved in methanol 20 mL, Pd/C 20 mg added, and the reaction stirred under hydrogen balloon for 6 h, then filtered through celite bed and washed with excess methanol. The organic layer was concentrated to get the crude 86 which was purified by flash chromatography using 100-200 mesh silica gel. The compound 86 was eluted at 25% ethyl acetate in hexane as half white coloured solid compound 6-methoxy-5-morpholino-2-(4-(trifluoromethyl)benzyl)-2,3-dihydro-1H-inden-1-one 86. 1HNMR (400 MHz, CDCl3) δ ppm 7.53 (d, 2H), 7.34 (d, 2H), 7.18 (s, 1H), 6.80 (s, 1H), 3.89 (m, 3H), 3.86 (m, 4H), 3.38 (m, 1H), 3.15 (m, 4H), 3.08 (m, 1H), 2.96 (m, 1H), 2.68 (m, 2H); MS (ESI) m/z 406.0 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09359315B2
出典データセットuspto-grants-2016_06
ORD IDord-04f735722c8149d3a553c06b0eda9406
出典メモuspto-grants-2016_06