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HRID 335708作成日:2026年10月24日

Potassium Phosphate, Tribasic → (S)-3,7-di(pyridin-3-yl)-5'H-spiro[chromeno[2,3-c]pyridine-5,4'-oxazol]-2'-amine

https://huagongshe.com/ja/reaction/335708

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Benzeneethanamine, alpha-methyl-, phosphate (1:1)HCID 62885—
反応物3-Pyridinylboronic acidHCID 2734378—
反応物(S)-7-bromo-3-chloro-5'H-spiro[chromeno[2,3-c]pyridine-5,4'-oxazol]-2'-amineHCID 58466134—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物(S)-3,7-di(pyridin-3-yl)-5'H-spiro[chromeno[2,3-c]pyridine-5,4'-oxazol]-2'-amineHCID 58466285—

反応条件

温度100 °C

反応手順

A glass microwave reaction vessel was charged with (S)-7-bromo-3-chloro-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine (32 mg, 0.087 mmol), potassium phosphate (55.6 mg, 0.262 mmol), Amphos (1.525 mg, 2.153 μmol) and 3-pyridylboronic acid (32.2 mg, 0.262 mmol) in dioxane (0.6 mL) and water (0.200 mL). The reaction mixture was stirred and heated in a microwave at 100° C. for 30 min. The reaction mixture was diluted with water (mL) and extracted with EtOAc (2×5 mL). The organic extract was washed with saturated NH4Cl (2×5 mL) and dried over MgSO4. The solution was filtered and concentrated in vacuo to give the crude material as a yellow solid. The crude material was absorbed onto a plug of silica gel and purified by silica gel chromatography (0-10% MeOH in DCM) to provide (S)-3,7-di(pyridin-3-yl)-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine as white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883782B2
出典データセットuspto-grants-2014_11
ORD IDord-dded776655274b719acb40dfe7852e3c
出典メモuspto-grants-2014_11