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HRID 2421246作成日:2026年10月25日

Potassium Phosphate, Tribasic → 1-{3,5-difluoro-4-[(phenylmethyl)oxy]phenyl}-4-[(phenylmethyl)oxy]-1H-indole

https://huagongshe.com/reaction/2421246

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物4-(phenylmethoxy)-1H-indoleHCID 88465—
反応物L-ProlineHCID 145742—
反応物4-Bromo-2,6-difluoro-1-(benzyloxy)benzeneHCID 14207641—
溶媒DimethylformamideHCID 6228—
生成物1-{3,5-difluoro-4-[(phenylmethyl)oxy]phenyl}-4-[(phenylmethyl)oxy]-1H-indoleHCID 59627928—

反応条件

温度140 °C

反応手順

4-[(phenylmethyl)oxy]-1H-indole (500 mg, 2.24 mmoL), 4-bromo-2,6-difluorophenyl phenylmethyl ether (prepared as described in part a), 559 mg, 1.87 mmoL), K3PO4 (990 mg, 4.67 mmoL) and L-Proline (43 mg, 0.373 mmoL) were dissolved in DMF (5 mL) in a microwave vial and degassed by sonication under a flow of argon. To this was added CuI (71 mg, 0.373 mmoL) and the solution was heated to 140° C. in the microwave reactor. After 3 hours the mixture was partitioned between ethyl acetate (100 mL)/water (100 mL), the phases were separated and the aqueous phase re-extracted with ethyl acetate (100 mL). The combined organic phases were washed with sat. NH4Cl (2×100 mL), water (100 mL) and brine (2×100 mL) and finally dried over MgSO4. The crude product was purified by flash chromatography (Biotage SP4, 40+S Cartridge) eluting with a gradient of 0 to 20% Et2O in hexane to give the title compound (D21), (299 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07956083B2
出典データセットuspto-grants-2011_06
ORD IDord-21b4da8f52ec452fbd78b8ee88eef7e4
出典メモuspto-grants-2011_06