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HRID 1023643作成日:2026年10月26日

N,N'-Dimethylethylenediamine → 10-[(R)-4-(2,2,2-trifluoro-1-hydroxy-ethyl)-phenyl]-1,4-dioxa-10-aza-dispiro[4.2.4.2]tetradecan-9-one

https://huagongshe.com/reaction/1023643

反応式

関与物質

役割名称HCID仕込み量
反応物N,N'-DimethylethylenediamineHCID 8070—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物1,4-Dioxa-10-azadispiro[4.2.4.2]tetradecan-9-oneHCID 58230108—
反応物2,2,2-Trifluoro-1-(4-iodophenyl)ethanolHCID 59440865—
反応物(R)-2,2,2-trifluoro-1-(4-iodophenyl)ethanolHCID 68227618—
溶媒DimethylformamideHCID 6228—
生成物10-[(R)-4-(2,2,2-trifluoro-1-hydroxy-ethyl)-phenyl]-1,4-dioxa-10-aza-dispiro[4.2.4.2]tetradecan-9-oneHCID 5823010364.6%

反応条件

温度80 °C

反応手順

1,4-Dioxa-10-aza-dispiro[4.2.4.2]tetradecan-9-one (352 mg, obtained in example 133, step 3) was dissolved in DMF (22 mL) at RT. Then, (R)-2,2,2-trifluoro-1-(4-iodophenyl)ethanol (755 mg, for synthesis see: J. Org. Chem. 2009, 74, 1605-1610), N,N′-dimethylethylenediamine (sym) (294 mg), cuprous iodide (476 mg) and K3PO4 (1.06 g) were added to the reaction mixture. The mixture was heated to 80° C. for 4.5 hours. The reaction mixture was cooled down to 30° C. and more 2,2,2-trifluoro-1-(4-iodophenyl)ethanol (252 mg) was added. The mixture was re-heated to 80° C. for 2 hours. The reaction mixture was cooled, poured into ice/water and extracted two times with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered and the solvent was evaporated. The residue was purified by flash chromatography (silica gel, gradient of ethyl acetate in heptane) to give the title compound as a colorless solid (415 mg, 62%). MS (ESI): 386.4 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08722721B2
出典データセットuspto-grants-2014_05
ORD IDord-e4dede784b1d45d1add7db7199971c82
出典メモuspto-grants-2014_05