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HRID 11915作成日:2026年10月26日

Sodium Carbonate → (R)-4,6-Dimethyl-3,4-dihydro-1H-2,4a,5-triaza-fluorene-2-carboxylic Acid Tert-butyl Ester

https://huagongshe.com/reaction/11915

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Sodium HydroxideHCID 14798—
反応物TrimethylboroxineHCID 574072—
反応物(4R)-6-bromo-4-methyl-3,4-dihydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl esterHCID 86590112—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物(R)-4,6-Dimethyl-3,4-dihydro-1H-2,4a,5-triaza-fluorene-2-carboxylic Acid Tert-butyl EsterHCID 6935751671.1%

反応手順

To a solution of 0.20 g (0.55 mmol) (R)-6-bromo-4-methyl-3,4-dihydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester (Example 5, intermediate a) in 10 ml 1,2-dimethoxyethane was added 63 mg (55 μmol) tetrakis(triphenylphosphine)palladium. After 30 min, 5 ml saturated aqueous sodium carbonate solution and 0.09 ml (0.65 mmol) of a 1M trimethylboroxine solution in THF were added and the resulting suspension was heated to reflux for 5 h. The reaction mixture was cooled to room temperature, poured into 20 ml 1M aqueous sodium hydroxide solution and extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash column chromatography on silica gel (0.032–0.063 mm) with ethyl acetate:n-hexane (1:1) as eluant to yield the desired product as a yellow solid (71.1%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098337B2
出典データセットuspto-grants-2006_08
ORD IDord-45ca063676444665b7e575b5a775cc21
出典メモuspto-grants-2006_08