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HRID 1406739作成日:2026年10月24日

Potassium Carbonate → (2,4-Bis-benzyloxy-5-isopropyl-phenyl)-[5-2-methoxy-ethoxy-1,3-dihydro-isoindol-2-yl]-methanone

https://huagongshe.com/ja/reaction/1406739

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2-Chloroethyl methyl etherHCID 12316—
反応物(2,4-Bis-benzyloxy-5-isopropyl-phenyl)-(5-hydroxy-1,3-dihydro-isoindol-2-yl)-methanoneHCID 66672264—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物(2,4-Bis-benzyloxy-5-isopropyl-phenyl)-[5-2-methoxy-ethoxy-1,3-dihydro-isoindol-2-yl]-methanoneHCID 59263156104.2%

反応手順

(2,4-Bis-benzyloxy-5-isopropyl-phenyl)-(5-hydroxy-1,3-dihydro-isoindol-2-yl)-methanone (A2 from 2,4-bis-benzyloxy-5-isopropyl-benzoic acid (Preparation B10) and 5-hydroxyisoindoline) (100 mg, 0.2 mmol), 1-chloro-2-methoxy-ethane (23.6 mg, 0.25 mmol) and K2CO3 (34.5 mg, 0.25 mmol) in DMF (4 ml) were combined and stirred for 2 hours at room temperature. A further 0.25 mmol of 1-chloro-2-methoxy-ethane and K2CO3 was added then heated at 90° C. for 16 hours. Reaction cooled to room temperature and diluted with EtOAc then filtered. The filtrate was reduced in vacuo then purified by flash column chromatography, eluting with 100% petroleum ether to 100% ethyl acetate to afford 115 mg of the title compound as a colourless gel. MS: [M+H]+ 552

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08916552B2
出典データセットuspto-grants-2014_12
ORD IDord-1e5afa0e08424384a6eb46f81a9cf65f
出典メモuspto-grants-2014_12