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HRID 216904作成日:2026年10月27日

Potassium Carbonate → (S)-tert-butyl 4-(1-amino-1-oxo-3-(4'-(trifluoromethyl)biphenyl-4-yl)propan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate

https://huagongshe.com/reaction/216904

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
反応物4-(Ethylsulphonyl)benzeneboronic acidHCID 2773420—
反応物(S)-tert-Butyl 4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 59568595—
溶媒AcetonitrileHCID 6342—
生成物(S)-tert-butyl 4-(1-amino-1-oxo-3-(4'-(trifluoromethyl)biphenyl-4-yl)propan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 59568598—
生成物(S)-tert-butyl 4-(1-amino-3-(4'-(ethylsulfonyl)biphenyl-4-yl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 59568601—

反応条件

温度75 °C

反応手順

(S)-tert-Butyl 4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate (Example 1, step (iii), 2.0 g) in acetonitrile (5 mL) under nitrogen was treated with 4-(trifluoromethyl)phenylboronic acid (0.367 g) and 4-(ethylsulfonyl)phenylboronic acid (0.414 g) followed by aqueous potassium carbonate (3.87 mL) and 1,1 bis(di-tert-butylphosphino)ferrocene palladium dichloride (25 mg). The mixture was stirred at 75° C. for 18 h. The reaction mixture was evaporated, dissolved in dichloromethane, evaporated onto silica and purified on a silica column eluting with 50% ethyl acetate in isohexane and then 100% ethyl acetate to afford (S)-tert-butyl 4-(1-amino-1-oxo-3-(4′-(trifluoromethyl)biphenyl-4-yl)propan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate and (S)-tert-butyl 4-(1-amino-3-(4′-(ethylsulfonyl)biphenyl-4-yl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate as a mixture (1.7 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193239B2
出典データセットuspto-grants-2012_06
ORD IDord-5e10018b5c9a4bfea64f98faff99416e
出典メモuspto-grants-2012_06