참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dabco | HCID 9237 | — |
| 반응물 | 4-Aminopyrimidine | HCID 68958 | — |
| 반응물 | 5-Chloro-2,4-difluorobenzenesulphonyl chloride | HCID 2773527 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 5-chloro-2,4-difluoro-N-pyrimidin-4-ylbenzenesulfonamide | HCID 59436545 | 5% |
반응 단계
A mixture of 4-aminopyrimidine (1.30 g, 13.7 mmol) and 1,4-diazabicyclo[2.2.2]octane (1.54 g, 13.7 mmol) were added concurrently to a solution of 5-chloro-2,4-difluorobenzenesulfonyl chloride (3.4 g, 14 mmol) in anhydrous acetonitrile (63 mL). The reaction mixture immediately turned yellow and a precipitate formed. The reaction mixture was stirred under argon. After 72 hours, the reaction mixture was filtered and the filtrate was concentrated in vacuo to give a residue. The residue was partitioned between 1M hydrochloric acid and ethyl acetate. The organic phase was separated, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was partially purified by automated flash column chromatography using an 80 g silica gel ISCO™ column using hexanes to 1% v/v acetic acid in ethyl acetate gradient elution. The product was purified a second time by reverse phase HPLC to give the title compound (193 mg, 5%) as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08541588B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-e411c3715dc34aff853b7427251500dc |
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| 출처 메모 | uspto-grants-2013_09 |
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