참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanesulfonamide | HCID 72879 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Propylphosphonic anhydride | HCID 111923 | — |
| 반응물 | 2,4,5-Trifluorobenzoic acid | HCID 521170 | — |
| 반응물 | N,N-dimethylformamide ethyl acetate | HCID 22989253 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2,4,5-trifluoro-N-(methylsulfonyl)benzamide | HCID 58042435 | 72% |
반응 단계
2,4,5-Trifluorobenzoic acid (3.00 g, 17.0 mmol), N-ethyl-N-isopropylpropan-2-amine (8.9 mL, 6.6 g, 51.1 mmol), 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphorinane-2,4,6-trioxide 50% solution in EtOAc/DMF (12.7 mL, 13.6 g, 42.6 mmol) and methanesulfonamide (3.24 g, 34.1 mmol) were suspended in THF (40 mL) and stirred under a nitrogen atmosphere at reflux for 18 hours. The reaction mixture was cooled, concentrated in vacuo and the residue suspended in water (pH=4). The mixture was acidified to pH=2 with an aqueous solution of potassium hydrogen sulfate (0.5 M). The mixture was extracted with EtOAc (1×100 mL). The organic layer was washed with brine (2×50 mL), dried over sodium sulfate, filtered and evaporated to yield the crude solid. The crude solid was triturated with hexane to yield the title compound as an off-white crystalline solid (3.08 g, 72%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09102621B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-ae3ee945d1d34237a7f0a936d30ca45a |
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| 출처 메모 | uspto-grants-2015_08 |
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