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HRID 75440作成日:2026年10月25日

Triethylamine → 3-(2,6-Dichloro-5-nitropyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octane

https://huagongshe.com/reaction/75440

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2,4,6-Trichloro-5-nitropyrimidineHCID 4297843—
反応物8-Oxa-3-aza-bicyclo(3.2.1)octane hydrochlorideHCID 21983536—
溶媒DichloromethaneHCID 6344—
生成物3-(2,6-Dichloro-5-nitropyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octaneHCID 86665896—

反応条件

温度0 °C

反応手順

2,4,6-Trichloro-5-nitropyrimidine (45, 1.43 g, 6.26 mmoles) was dissolved in dichloromethane and cooled to 0° C. A solution of 8-oxa-3-azabicyclo[3.2.1]octane (2, 0.934 g, 6.26 mmoles) in dichloromethane and triethylamine (0.873 mL, 6.26 mmoles) was slowly added over 1 hour. The solution was allowed to stir at 0° C. for 2 hours, then warmed to room temperature and stirred for an additional 16 hours. The reaction mixture was filtered, the filtrate was concentrated, dissolved in ethyl acetate, washed with 1N hydrochloric acid, saturated sodium bicarbonate, brine, dried, and concentrated to provide 3-(2,6-dichloro-5-nitropyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octane (46). Yield: 1.53 g (80%). HRMS; [M+H]+ Obs'd=305.0200, [M+H]+ Calc'd=305.0203.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835429B2
出典データセットuspto-grants-2014_09
ORD IDord-7de2637b233449baa3af76c79335ccfc
出典メモuspto-grants-2014_09