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HRID 58763作成日:2026年10月26日

Sodium Carbonate → 5-(2,5-difluorobenzyl)-N-(2-(5-phenyl-1H-indol-3-yl)ethyl)isoxazole-3-carboxamide

https://huagongshe.com/reaction/58763

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物Phenylboronic AcidHCID 66827—
反応物N-(2-(5-bromo-1H-indol-3-yl)ethyl)-5-(2,5-difluorobenzyl)isoxazole-3-carboxamideHCID 66831747—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物5-(2,5-difluorobenzyl)-N-(2-(5-phenyl-1H-indol-3-yl)ethyl)isoxazole-3-carboxamideHCID 668319976%

反応手順

A mixture of benzene boronic acid (0.023 g; 0.191 mmol), N-(2-(5-bromo-1H-indol-3-yl)ethyl)-5-(2,5-difluorobenzyl)isoxazole-3-carboxamide (0.080 g; 0.174 mmol), tetrakis(triphenylphosphine)palladium(0) (0.020; 0.017 mmol) and sodium carbonate (0.037 g; 0.347 mmol) in DME (3 mL) and water (1 mL) was irradiated in the microwave oven at 130° C. for 20 minutes, the resulting solution was partitioned between water and EA, the organic layer was concentrated under reduced pressure. The crude mixture was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) and by preparative HPLC method 2 to yield 0.0048 g (6%) of 5-(2,5-difluorobenzyl)-N-(2-(5-phenyl-1H-indol-3-yl)ethyl)isoxazole-3-carboxamide as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434722B2
出典データセットuspto-grants-2016_09
ORD IDord-e29351ed4cb74c2f91c7b20c6c6e0e19
出典メモuspto-grants-2016_09