참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | P-Toluenesulfonamide | HCID 6269 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2,3-Bis-bromomethyl-1,4-difluorobenzene | HCID 59382290 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4,7-Difluoro-2-(toluene-4-sulfonyl)isoindoline | HCID 59382248 | 56% |
반응 단계
A solution of 4-toluenesulphonamide (2.44 g, 14.28 mmol) in N,N-dimethylformamide (10 ml) was added dropwise to a vigourously stirred suspension of sodium hydride (1.2 g, 60 wt % in mineral oil, 30.0 mmol) in anhydrous N,N-dimethylformamide (60 ml). The mixture was stirred at room temperature for 1 hour, at 110° C. for 1 hour and was then cooled to 60° C. and a solution of 2,3-bis-bromomethyl-1,4-difluorobenzene (4.28 g, 14.28 mmol) in N,N-dimethylformamide (30 ml) was added dropwise. The mixture was stirred at 60° C. for 1 hour and then at room temperature for 16 hours. The solvent was removed in vacuo and the residue partitioned between dichloromethane and 1M hydrochloric acid. The organic layer was separated, washed with 5% aqueous potassium carbonate solution, the organics were separated and the solvent removed in vacuo. The residue was rinsed with diethyl ether, filtered and the solids sucked dry under reduced pressure to afford 4,7-difluoro-2-(toluene-4-sulfonyl)isoindoline (2.46 g, 56%) as a pale tan solid. 1H NMR (DMSO-d6) 7.82 (2H, d), 7.43 (2H, d), 7.15 (2H, dd), 4.66 (4H, s), 2.36 (3H, s). MS: [M+H]+ 310.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08530469B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-28f6d75c693543f6ad7c911c7f8a0896 |
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| 출처 메모 | uspto-grants-2013_09 |
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