関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Benzonitrile, 2-((3-oxo-1-cyclohexen-1-yl)amino)- | HCID 184360 | — |
| 反応物 | 5-Chloro-2-(3-oxocyclohexen-1-yl)aminobenzonitrile hydrochloride | HCID 20037714 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 9-Amino-7-chloro-3,4-dihydroacridin-1(2H)-one | HCID 13756057 | 4.3% |
反応手順
In 5 liters of toluene were combined 200 ml of dimethylformamide, 180.71 g of 5-chloro-2-(3-oxocyclohexen-1-yl)aminobenzonitrile hydrochloride prepared in the same manner as the compounds of EXAMPLES 1 and 2, 176 g (2 eq) of milled K2CO3 and 3 g of cuprous chloride (CuCl). After 6 hours of reflux 3 g more of CuCl was added. After 12 hours of reflux 3 g more of CuCl was added. After overnight reflux the reaction mixture was evaporated and the residue extracted with dichloromethane via a Soxhlet extraction apparatus for 12 hours. The dichloromethane solution was evaporated to a solid. The solid was suspended in water and H2SO4 was added. The resultant salt which precipitated out was filtered and made basic with 10% NaOH. The solid was filtered and recrystallized twice from isopropanol/toluene to yield 6.84 g (4%) of a solid, melting point over 260° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04754050 |
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| 出典データセット | uspto-grants-1988_06 |
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| ORD ID | ord-efe7fdd9d5364a3581efc5f7ce02ff30 |
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| 出典メモ | uspto-grants-1988_06 |
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