참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl 2,4-Difluorobenzoate | HCID 2782897 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | 6-(Benzyloxy)pyridin-3-ol | HCID 42553041 | — |
| 용매 | 2-Methyltetrahydrofuran | HCID 7301 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Methyl 2-(6-(benzyloxy)pyridin-3-yloxy)-4-fluorobenzoate | HCID 67228431 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09303025B2 |
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| 출처 데이터셋 | uspto-grants-2016_04 |
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| ORD ID | ord-75b847cf353f4de0b04265aa3c78dc54 |
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| 출처 메모 | uspto-grants-2016_04 |
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