참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Ether | HCID 8254 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | DCM MeOH AcOH | HCID 21877243 | — |
| 반응물 | [5-(4-Fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid methyl ester | HCID 69522849 | — |
| 용매 | MeOH tetrahydrofuran | HCID 21899815 | — |
| 생성물 | [5-(4-Fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid | HCID 21087356 | 16.3% |
반응 단계
To a solution of [5-(4-fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid methyl ester (prepared above, 82 mg, 0.269 mmol) in THF/methanol (6 mL/0.3 mL) was added 1 N NaOH (0.3 mL, 0.3 mmol). Additional 1 N NaOH aliquots were added after 5 min (0.15 mL), 25 min (0.25 mL), and 2 h (1.0 mL). By thin layer chromatography (15/84/1 methanol/dichloromethane/acetic acid) it appeared that the starting material never disappeared, but LC/MS showed the presence of mostly methyl ether, with some desired acid and no starting material. The reaction mass was extracted with ethyl acetate. The combined organic layers were washed 1× with water, then 2× with 5% NaHCO3. The aqueous layers were combined, acidified to pH 1 with 3% HCl and extracted with dichloromethane. The organic layers were combined, washed with brine, dried and concentrated in vacuo to afford 12.8 mg (16% yield) of the titled carboxylic acid as a white solid. ESI-MS m/z 292 (MH+), 290 (M−H)−.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07176310B1 |
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| 출처 데이터셋 | uspto-grants-2007_02 |
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| ORD ID | ord-dd9c924abb3f41efa2bd2e05fc07d16b |
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| 출처 메모 | uspto-grants-2007_02 |
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