関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Asenapine | HCID 163091 | — |
| 反応物 | Maleic Acid | HCID 444266 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Asenapine Maleate | HCID 6917875 | 84,144.102% |
反応手順
To 91.0 g (0.32 mmol) of the purified trans-5-chloro-2,3,3a,12b-tetrahydro-2-methyl-1H-dibenzo[2,3;6,7]-oxepino[4,5-c]pyrrole obtained in Production Example 2 there were added 310 mL of 99.5% ethanol and 40.6 g (0.35 mol) of maleic acid, and the obtained mixture was heated to 60° C. to obtain a homogeneous solution. The solution was cooled to −10° C. over a period of 18 hours. The precipitated crystals were separated off by filtration, and the crystals were washed with 45 mL of cold ethanol and dried to obtain 108.2 g of trans-5-chloro-2,3,3a,12b-tetrahydro-2-methyl-1H-dibenzo[2,3;6,7]-oxepino[4,5-c]pyrrole maleate as a white solid. The yield was 84.6%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08288564B2 |
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| 出典データセット | uspto-grants-2012_10 |
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| ORD ID | ord-678290f633a8454ea83d7866956a888d |
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| 出典メモ | uspto-grants-2012_10 |
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