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HRID 603926作成日:2026年10月27日

Triethylamine → {4-[(2R,3R)-3-{[2-(1,3-benzodioxol-5-yl)-2-oxoethyl]thio}-1-(4-chlorophenyl)-4-oxoazetidin-2-yl]phenoxy}acetic acid

https://huagongshe.com/reaction/603926

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物TriphenylphosphineHCID 11776—
反応物1-(1,3-Dioxaindan-5-yl)-2-bromoethan-1-oneHCID 243777—
反応物tert-Butyl (4-{(2R,3R)-1-(4-chlorophenyl)-3-[(3-nitropyridin-2-yl)dithio]-4-oxoazetidin-2-yl}phenoxy)acetateHCID 86643081—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物{4-[(2R,3R)-3-{[2-(1,3-benzodioxol-5-yl)-2-oxoethyl]thio}-1-(4-chlorophenyl)-4-oxoazetidin-2-yl]phenoxy}acetic acidHCID 67270870—

反応手順

tert-Butyl (4-{(2R,3R)-1-(4-chlorophenyl)-3-[(3-nitropyridin-2-yl)dithio]-4-oxoazetidin-2-yl}phenoxy)acetate (Method 27) (0.70 g, 1.22 mmol) was dissolved in acetone (30 mL) at room temperature, then water (10 mL) and triphenyl phosphine (0.32 g, 1.22 mmol) was added. The mixture was stirred at room temperature for 15 minutes and then concentrated under reduced pressure to afford the crude thiol as a brown oil. This crude thiol was immediately dissolved in CH2Cl2 (30 mL) and 1-benzo[1,3]dioxol-5-yl-2-bromo-ethanone (0.59 g, 2.44 mmol) was added, followed by Et3N (0.34 mL, 2.44 mmol). The mixture was stirred at room temperature for 18 hours, concentrated under reduced pressure and purified by flash-chromatography (Heptane:EtOAc 7:3 and then 2:1). The resulting product (0.90 g) was dissolved in 15 ml formic acid and stirred at room temperature for 3 hours. Concentration under reduced pressure and purification by flash-chromatography afforded the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07906502B2
出典データセットuspto-grants-2011_03
ORD IDord-d33d4c7d09b5497fabebe5f35fbcdc9e
出典メモuspto-grants-2011_03