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HRID 915050作成日:2026年10月26日
Dichloromethane → 6-{6-bromo-5-[(dimethyl-lambda~4~-sulfanylidene)amino]-3-phenyl-2-pyrazinyl}-2-isopropyl-3 (2H)-pyridazinone
https://huagongshe.com/reaction/915050
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| 反応物 | 6-(5-amino-6-bromo-3-phenyl-2-pyrazinyl)-2-isopropyl-3(2H)-pyridazinone | HCID 86600915 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 生成物 | 6-{6-bromo-5-[(dimethyl-lambda~4~-sulfanylidene)amino]-3-phenyl-2-pyrazinyl}-2-isopropyl-3 (2H)-pyridazinone | HCID 87798659 | — |
反応手順
To a solution of DMSO (0.75 ml) in CH2Cl2 (5 ml) was added trifluoromethanesulfonic anhydride (1.5 ml) dropwise at <−75° C. under nitrogen. A suspension of 6-(5-amino-6-bromo-3-phenyl-2-pyrazinyl)-2-isopropyl-3(2H)-pyridazinone (3.00 g) in a mixture of DMSO (5 ml) and CH2Cl2 (6 ml) was added and stirred at −65° C. for 2 hours and at −55° C. for one hour. The reaction mixture was quenched with 1N aq. NaOH (20 ml) and stirred at 15° C. for 10 minutes. An organic layer was collected, dried over MgSO4 and concentrated under reduced pressure to give a solid. The solid was suspended in acetone and collected by filtration to give 6-{6-bromo-5-[(dimethyl-lambda˜4˜-sulfanylidene)amino]-3-phenyl-2-pyrazinyl}-2-isopropyl-3(2H)-pyridazinone (3.16 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07265120B2 |
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| 出典データセット | uspto-grants-2007_09 |
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| ORD ID | ord-38ecb570399c4ff8acabdb50667aacbb |
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| 出典メモ | uspto-grants-2007_09 |
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