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HRID 1625355作成日:2026年10月26日

Bis(2-chloroethyl) ether → (2,4-Bis-benzyloxy-5-isopropyl-phenyl)-(5-morpholin-4-yl-1,3-dihydro-isoindol-2-yl)-methanone

https://huagongshe.com/reaction/1625355

反応式

関与物質

役割名称HCID仕込み量
反応物Bis(2-chloroethyl) etherHCID 8115—
反応物DiisopropylethylamineHCID 81531—
反応物(5-Amino-1,3-dihydro-isoindol-2-yl)-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-methanoneHCID 66672407—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物(2,4-Bis-benzyloxy-5-isopropyl-phenyl)-(5-morpholin-4-yl-1,3-dihydro-isoindol-2-yl)-methanoneHCID 59263147—

反応条件

温度150 °C

反応手順

A mixture of (5-amino-1,3-dihydro-isoindol-2-yl)-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-methanone (100 mg; 0.2 mmol), bis(2-chloroethyl)ether (30 μl; 1.1 equiv.), Hunigs base (125 μl; 3.5 equiv.) and tetrabutylammonium iodide (10 mg) in NMP (1 ml) was heated in a CEM microwave synthesiser at 150° C. for 30 minutes. A further 30 μl of Hunig's base and 125 μl of bis(2-chloroethyl)ether were added and heating repeated for the same time. The reaction mixture was partitioned between EtOAc and saturated NH4Cl solution, the EtOAc layer was separated, washed with more saturated NH4Cl solution, then brine, dried (MgSO4) and evaporated. Purification by flash column chromatography (1:2 then 1:1 then 2:1 EtOAc/P.E. as eluant) gave 60 mg of (2,4-bis-benzyloxy-5-isopropyl-phenyl)-(5-morpholin-4-yl-1,3-dihydro-isoindol-2-yl)-methanone. MS: [M+H]+ 563.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08779132B2
出典データセットuspto-grants-2014_07
ORD IDord-3fe8af73e93548cc8ddf16af07de45aa
出典メモuspto-grants-2014_07