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HRID 404483作成日:2026年10月25日

Triethylamine → ((2S,5R)-1-(4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-6-(4-nitrophenyl)-1,3,5-triazin-2-yl)pyrrolidine-2,5-diyl)dimethanol

https://huagongshe.com/reaction/404483

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-Oxa-8-azabicyclo(3.2.1)octane hydrochlorideHCID 53401129—
反応物HCID 86636521HCID 86636521—
溶媒EthanolHCID 702—
生成物((2S,5R)-1-(4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-6-(4-nitrophenyl)-1,3,5-triazin-2-yl)pyrrolidine-2,5-diyl)dimethanolHCID 67021926—

反応条件

温度130 °C

反応手順

A suspension of ((2S,5R)-1-(4-chloro-6-(4-nitrophenyl)-1,3,5-triazin-2-yl)pyrrolidine-2,5-diyl)dimethanol (0.91 g, 2.5 mmol), 3-oxa-8-azabicyclo[3.2.1]octane hydrochloride (0.37 g, 2.5 mmol) in ethanol (13 mL) was treated with triethylamine (1 mL) and heated in a microwave reactor for 20 minutes at 130° C. The reaction mixture was purified by automated flash chromatography (methanol/chloroform) to provide the title compound as a hard peach colored foam. MS (ES+)=443.2 (M+H)+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08748421B2
出典データセットuspto-grants-2014_06
ORD IDord-f3f5d48c603d42f0b930208d09982b2a
出典メモuspto-grants-2014_06