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HRID 48515作成日:2026年10月25日

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

https://huagongshe.com/reaction/48515

反応式

関与物質

役割名称HCID仕込み量
反応物AzetidineHCID 10422—
反応物Binap, (A+-)-HCID 634876—
反応物Sodium t-butoxideHCID 23676156—
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Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-(-)-5'-(1-Azetidinyl)spiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[2,3-b]pyridine]HCID 53881099—

反応条件

温度75 °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), azetidine (0.101 mL, 1.5 mmol), sodium tert-butoxide (135 mg, 1.4 mmol), tris(dibenzylideneacetone)dipalladium (46 mg, 0.05 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (62 mg, 0.1 mmol) and anhydrous tetrahydrofuran (9 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 75° C. for 4 hours, cooled to room temperature, dissolved in chloroform (20 mL), washed with brine (3×10 mL), dried (MgSO4), evaporated under reduced pressure, and purified by flash chromatography through silica gel (eluting with ammoniated chloroform/methanol 95:5) to procure the title compound (230 mg, 0.0.85 mmol, 85%) as a light tan solid: chemical ionization MS (m/z, relative intensity) 272 ([MH]+, 56).

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-4877672a9abd4bf59aa60d382fd66bf6
出典メモuspto-grants-2004_03