戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 48517作成日:2026年10月25日

Triethylamine → (R)-(-)-5'-(2-Trimethylsilylethynyl)spiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[2,3-b]pyridine]

https://huagongshe.com/reaction/48517

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物TrimethylsilylacetyleneHCID 66111—
反応物(2R)-5'-bromo-3'H-spiro[4-azabicyclo[2.2.2]octane-2,2'-furo[2,3-b]pyridine]HCID 54506690—
触媒HCID 178418397HCID 178418397—
溶媒AcetonitrileHCID 6342—
生成物(R)-(-)-5'-(2-Trimethylsilylethynyl)spiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[2,3-b]pyridine]HCID 5435774190%

反応条件

温度100 °C

反応手順

(R)-(−)-5′-Bromospiro[1-azabicyclo[2.2.2]octane-3,2′(3′H)-furo[2,3-b]pyridine](295 mg, 1 mmol), trimethylsilylacetylene (0.355 mL, 2.5 mmol), tetrakis(triphenylphosphine)palladium (230 mg, 0.2 mmol), triethylamine (2 mL) and anhydrous acetonitrile (2 mL) were combined in a heavy-walled threaded glass tube containing a magnetic stir bar, purged with argon and sealed with a Teflon plug and FETFE O-ring. The mixture was stirred and heated at 100° C. for 4 hours, cooled to room temperature, dissolved in chloroform (25 mL), washed with saturated aqueous sodium carbonate (2 mL), dried (MgSO4), and evaporated under reduced pressure. Purification by flash chromatography through silica gel (eluting with ammoniated ether/methanol, 9:1) afforded the title compound (280 mg, 0.90 mmol, 90%): chemical ionization MS (m/z, relative intensity) 313 ([MH]+, 30).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703502B2
出典データセットuspto-grants-2004_03
ORD IDord-916899a19c28497e909a2862eb131f4d
出典メモuspto-grants-2004_03