関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Thiosulfate | HCID 24477 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 7-Amino-2-methyl-2,3-dihydro-1H-isoindol-1-one | HCID 45088712 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 7-Amino-4-bromo-2-methylisoindolin-1-one | HCID 53408459 | 74% |
反応手順
NBS (2.3 g, 12.96) was added to a cold (−8° C. to −10° C.) solution of 7-amino-2-methyl-2,3-dihydro-1H-isoindol-1-one (2 g, 12.4 mmol) in DCM (40 mL) and the mixture stirred at −8° C. to −10° C. for 1 h. A solution of 10% aq. sodium thiosulfate (30 mL) was then added to the reaction mixture and stirring was continued for another 20 minutes. The layers were separated and the aqueous layer was extracted with DCM (2×20 mL). The combined organic extracts were washed with water (3×40 mL) and brine (30 mL), and the organic layer was dried (Na2SO4) and concentrated in vacuo to yield 3.2 g of crude product. This material was triturated with ethyl acetate (10 mL) to give 2.2 g of pure 7-amino-4-bromo-2-methyl-2,3-dihydro-1H-isoindol-1-one (XXXIX, yield: 74%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09096624B2 |
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| 出典データセット | uspto-grants-2015_08 |
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| ORD ID | ord-dce05f2931924cd5b91ef7ab2c91aa50 |
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| 出典メモ | uspto-grants-2015_08 |
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