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HRID 1255840作成日:2026年10月26日

1,8-Diazabicyclo(5.4.0)undec-7-ene → 3-[(1S)-1-azidoethyl]-5-bromopyridine

https://huagongshe.com/reaction/1255840

反応式

関与物質

役割名称HCID仕込み量
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物(R)-1-(5-bromopyridin-3-yl)ethanolHCID 68655864—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物3-[(1S)-1-azidoethyl]-5-bromopyridineHCID 8664186075%

反応手順

To a solution of (1R)-1-(5-bromopyridin-3-yl)ethanol (10 mmol) in tetrahydrofuran (40 mL), cooled to 0° C., was added diphenylphosphoryl azide (4.3 mL, 20 mmol) in one portion followed by 1,8-diazabicyclo[5.4.0]undec-7-ene (3 mL, 20 mmol) dropwise over 30 minutes. After this time the reaction mixture was allowed to warm slowly to room temperature and was stirred overnight. The mixture was diluted with ethyl acetate (50 mL) and water (50 mL), the two phases separated and the aqueous phase extracted with ethyl acetate (3×50 mL). The combined organic phases were washed with brine (50 mL), dried (MgSO4) and concentrated under reduced pressure to give a black liquid which was purified by flash chromatography (silica, ethyl acetate/hexanes) to give 3-[(1S)-1-azidoethyl]-5-bromopyridine (1.7 g, 75%) as a colourless liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08461161B2
出典データセットuspto-grants-2013_06
ORD IDord-4db8b242fd664bfd922465040967c31a
出典メモuspto-grants-2013_06