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HRID 1043351作成日:2026年10月25日
N-methyl-2-pyrrolidone → 2,2'-(Disulphanediyldiethane-2,1-diyl)bis(6-chloro-1H-benzo[de]-isoquinoline-1,3(2H)-dione)
https://huagongshe.com/reaction/1043351
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 反応物 | 1H,3H-Naphtho[1,8-cd]pyran-1,3-dione, 6-chloro- | HCID 77672 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 2-[(2-Aminoethyl)disulfanyl]ethan-1-amine hydrochloride | HCID 167628 | — |
| 生成物 | 2,2'-(Disulphanediyldiethane-2,1-diyl)bis(6-chloro-1H-benzo[de]-isoquinoline-1,3(2H)-dione) | HCID 59428884 | — |
反応手順
9.30 g of 6-chloro-1H,3H-benzo[de]isochromene-1,3-dione and 4.46 g of hydrochlorided cystamine hydrochloride are suspended in 50 ml of N-methylpyrrolidone (NMP). 5.5 g of diisopropylethylamine are added and the mixture is heated with stirring at 120° C. After two hours, 50 ml of NMP are added and the mixture is kept with stirring at 120° C. for 3 hours. After cooling, the precipitated product is recovered and the filtered solution is extended by addition of 200 ml of water, and a second precipitate is recovered. The precipitates are washed with water and dried. 11.46 g of white powder are recovered. The analyses show that the product is in accordance with the expected product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08562693B2 |
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| 出典データセット | uspto-grants-2013_10 |
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| ORD ID | ord-5aac77b1d48a4e17893caa996dd2cbc7 |
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| 出典メモ | uspto-grants-2013_10 |
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