참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzenesulfonyl chloride | HCID 7369 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3-(1H-imidazol-2-yl)-1-(phenylsulfonyl)-1H-indole | HCID 57516836 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(phenylsulfonyl)-3-(1-(phenylsulfonyl)-1H-imidazol-2-yl)-1H-indole | HCID 57516837 | 40% |
반응 단계
To a solution of 3-(1H-imidazol-2-yl)-1-(phenylsulfonyl)-1H-indole (9ya) (20 mmol) in anhydrous THF (300 mL) at 0° C. was added sodium hydride (60% dispersion in mineral oil, 1.2 equiv, 24 mmol) and stirred for 20 min. Benzenesulfonyl chloride (1.2 equiv, 24 mmol) was added and the reaction mixture was stirred overnight. After dilution by 200 mL of saturated NaHCO3 solution (aqueous), the reaction mixture was extracted by ethyl acetate (600 mL). The organic layer was dried over magnesium sulfate and concentrated. The residue was purified by flash column chromatography (hexane:ethyl acetate 5:1) to give a white solid. Yield: 40%. 1H NMR (CDCl3, 300 MHz) δ 8.02-8.08 (m, 4H), 7.72 (d, J=1.5 Hz, 1H), 7.35-7.60 (m, 8H), 7.23 (d, J=1.5 Hz, 1H), 7.10-7.16 (m, 3H). MS (ESI) calcd for C23H17N3O4S2 463.1. found 486.0 [M+Na]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09447049B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-8ff8dc1d75a74b2392126e049a48f1bd |
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| 출처 메모 | uspto-grants-2016_09 |
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