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HRID 1970336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/1970336
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)pyrimidine | HCID 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 trifluoromethanesulfonate | HCID 86640726 | — |
| 溶媒 | Dimethylformamide | HCID 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-amine | HCID 58466271 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08426447B2 |
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| 出典データセット | uspto-grants-2013_04 |
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| ORD ID | ord-7f415de1f2ca4ca8adc05a1712cf81a8 |
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| 出典メモ | uspto-grants-2013_04 |
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