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HRID 1289880作成日:2026年10月25日
Cesium → 4,6-diethoxy-2-[1-phenyl-3-trifluoromethylpyrazol-5-yl-oxymethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide
https://huagongshe.com/reaction/1289880
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Cesium | HCID 5354618 | — |
| 反応物 | 2-chloromethyl-4, 6-diethoxy-1,2-benzisothiazol-3 (2H)-one 1,1-dioxide | HCID 53817436 | — |
| 反応物 | HCID 178516151 | HCID 178516151 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4,6-diethoxy-2-[1-phenyl-3-trifluoromethylpyrazol-5-yl-oxymethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide | HCID 18922609 | 714.4% |
反応手順
The cesium salt of 1-phenyl-3-trifluoromethyl-5-hydroxypyrazole [prepared from 1-phenyl-3-trifluoromethyl-5-hydroxypyrazole (0.714 g, 0.312 mmol) and Cs2CO3 (0.509 g, 0.156 mmol)] was suspended in DMF (20 ml) and treated with 2-chloromethyl-4, 6-diethoxy-1,2-benzisothiazol-3 (2H)-one 1,1-dioxide (0.5 g, 0.156 mmol). The reaction mixture was stirred at room temperature for 24 hours, then was poured onto ice-water and was extracted with ethyl acetate (300 mL). The organic layer was washed with water, then brine and then was dried over MgSO4. The solvent was removed and the residue was purified by flash chromatography on silica gel eluting with CH2Cl2 to afford 0.57 g (71%) of 4,6-diethoxy-2-[1-phenyl-3-trifluoromethylpyrazol-5-yl-oxymethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide (Formula I: R1 =Ph; R2 =CF3 ; R3 =H; R4 =OEt; R5 =6-OEt), m.p. 159°-160° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05750550 |
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| 出典データセット | uspto-grants-1998_05 |
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| ORD ID | ord-399c4c1aa3d745c9bb5eb7fcec06b478 |
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| 出典メモ | uspto-grants-1998_05 |
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