関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methyl 2,4-Difluorobenzoate | HCID 2782897 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | 6-(Benzyloxy)pyridin-3-ol | HCID 42553041 | — |
| 溶媒 | 2-Methyltetrahydrofuran | HCID 7301 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Methyl 2-(6-(benzyloxy)pyridin-3-yloxy)-4-fluorobenzoate | HCID 67228431 | — |
反応手順
To 6-(benzyloxy)pyridin-3-ol (1.10 g) in 2-methyltetrahydrofuran (20 mL) was added potassium t-butoxide (5.47 mL, 1.0M in tetrahydrofuran). After stirring for 15 minutes, methyl 2,4-difluorobenzoate (1.035 g) in 2-methyltetrahydrofuran (2 mL) was added and the reaction heated to 75° C. for 1 hour. The reaction was cooled, diluted with ethyl acetate (150 mL), washed with water (50 mL), brine (50 mL), dried over magnesium sulfate, filtered and concentrated. Silica gel chromatography (SF40-80 g) eluting with a gradient of 5% to 20% ethyl acetate/hexanes gave the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09029404B2 |
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| 出典データセット | uspto-grants-2015_05 |
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| ORD ID | ord-81af208bf7a94fb2b2b9fb56bc926999 |
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| 出典メモ | uspto-grants-2015_05 |
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