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HRID 133501作成日:2026年10月25日

1,1,1-Trifluoro-2,4-pentanedione → 2,2,2-trifluoro-1-[4-(4-methoxy-phenyl)-2-methyl-6,7-dihydro-5H-cyclopenta[4,5]thieno[2,3-b]pyridin-3-yl)-ethanone

https://huagongshe.com/reaction/133501

反応式

関与物質

役割名称HCID仕込み量
反応物1,1,1-Trifluoro-2,4-pentanedioneHCID 73943—
反応物3-(4-methoxybenzoyl)-4H,5H,6H-cyclopenta[b]thiophen-2-amineHCID 28337440—
触媒Sulfuric AcidHCID 1118—
溶媒Acetic AcidHCID 176—
生成物2,2,2-trifluoro-1-[4-(4-methoxy-phenyl)-2-methyl-6,7-dihydro-5H-cyclopenta[4,5]thieno[2,3-b]pyridin-3-yl)-ethanoneHCID 1154560628.4%

反応条件

温度100 °C

反応手順

To a stirred solution of 50 mg (0.18 mmol) (2-amino-5,6-dihydro-4H-cyclopenta[b]thiophen-3-yl)-(4-methoxy-phenyl)-methanone in 2 ml acetic acid was added 0.022 ml (0.18 mmol) of 1,1,1-trifluoro-pentane-2,4-dione and one drop of sulfuric acid. The mixture was then stirred at 100° C. for 10 minutes in a microwave and then concentrated in vacuo. Flash chromatography (heptane/ethyl acetate 9:1) afforded 20 mg (28%) 2,2,2-trifluoro-1-[4-(4-methoxy-phenyl)-2-methyl-6,7-dihydro-5H-cyclopenta[4,5]thieno[2,3-b]pyridin-3-yl)-ethanone as a white solid. ES-MS m/e (%): 392 (M+H+, 100).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390903B2
出典データセットuspto-grants-2008_06
ORD IDord-38317f5fcbc64e05a0bb1813b07518c1
出典メモuspto-grants-2008_06