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HRID 335744作成日:2026年10月26日

Benzeneethanamine, alpha-methyl-, phosphate (1:1) → (R)-7'-(3,6-dihydro-2H-pyran-4-yl)-3'-fluoro-2'-(pyrimidin-5-yl)-5H-spiro[oxazole-4,9'-xanthen]-2-amine

https://huagongshe.com/reaction/335744

反応式

関与物質

役割名称HCID仕込み量
反応物Benzeneethanamine, alpha-methyl-, phosphate (1:1)HCID 62885—
反応物5-(Tributylstannyl)pyrimidineHCID 2763249—
反応物(R)-2-amino-2'-(3,6-dihydro-2H-pyran-4-yl)-6'-fluoro-5H-spiro[oxazole-4,9'-xanthene]-7'-yl trifluoromethanesulfonateHCID 86640726—
溶媒DimethylformamideHCID 6228—
生成物(R)-7'-(3,6-dihydro-2H-pyran-4-yl)-3'-fluoro-2'-(pyrimidin-5-yl)-5H-spiro[oxazole-4,9'-xanthen]-2-amineHCID 58466271—

反応条件

温度130 °C

反応手順

A mixture of 5-(tributylstannyl)pyrimidine (73.8 mg, 0.200 mmol), AmPhos (4.24 mg, 5.99 μmol) and (R)-2-amino-2′-(3,6-dihydro-2H-pyran-4-yl)-6′-fluoro-5H-spiro[oxazole-4,9′-xanthene]-7′-yl trifluoromethanesulfonate (50 mg, 0.100 mmol) in 0.3 mL of DMF was heated at 130° C. for 1 hour. After cooling and evaporation of the solvent under high vacuum, the mixture was purified by silica gel chromatography (DCM to DCM/EA=1:1 to 1:2 to pure EA to EA/MeOH=100:5 to 100:10) to provide (R)-7′-(3,6-dihydro-2H-pyran-4-yl)-3′-fluoro-2′-(pyrimidin-5-yl)-5H-spiro[oxazole-4,9′-xanthen]-2-amine as an off-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-83c10385655c4916ac2733575dba14e4
出典メモuspto-grants-2014_11