関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Aminophenol | HCID 403 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Pivaloyl chloride | HCID 62493 | — |
| 反応物 | Retinoic Acid | HCID 444795 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Fenretinide | HCID 5288209 | 123.4% |
反応手順
To a 5-Liter 4 neck round bottom flask equipped with a mechanical stirrer, temperature probe, addition funnel, and nitrogen inlet adapter was added 100.0 grams (333.3 mmol) of retinoic acid and 1.0 liter of ethyl acetate (EtOAc). The slurry was cooled to an internal temperature of 5° C. Triethylamine (50.7 milliliters, 366 mmol) was added all at once via graduated cylinder. To the thin slurry was then added trimethylacetyl chloride (45.1 milliliters, 366 mmol) via addition funnel over 23 minutes at an internal temperature of less than 5° C. After 3.5 hours, the reaction was judged to be complete by HPLC analysis. To the bright yellow slurry of the mixed anhydride was added a thin suspension of 4-aminophenol (76.3 grams, 700 mmol) in 500 milliliters of pyridine over 30 minutes at an internal temperature of 3-5° C. After 2 hours, the reaction was judged to be complete by HPLC analysis. To the slurry was added 500 milliliters of water over 10 minutes at an internal temperature of 4-8° C. After stirring for 30 minutes the layers were separated and the aqueous layer was extracted with 500 milliliters of EtOAc. The combined organic layers were washed with 3M HCl (3×700 milliliters). The pH of the last wash was 1-2 as determined by pH paper. The organic layer was then washed with 30% aqueous K2CO3 (3×600 milliliters) and brine (2×600 milliliters). The organic layer was held overnight at 0-10° C. The next morning the solution was dried with 50 grams of Na2SO4. After filtration of the drying salts, the amber solution was concentrated to a final volume of about 250 milliliters via rotary evaporation at an external temperature of 45-50° C. The thick slurry was allowed to cool to ambient temperature and 700 milliliters of heptane was added via addition funnel over about 45 minutes. The slurry was cooled to an internal temperature of 0-5° C. and held at this temperature for about 2 hours. The slurry was filtered and washed with a 0-10° C. 5/1 (v/v) mixture of heptane/EtOAc (1×200 milliliters, 1×150 milliliters) to give 161 grams of crude fenretinide wet cake (LOD=25%, 93% yield based on LOD, 98% pure by area percent).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07321064B1 |
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| 出典データセット | uspto-grants-2008_01 |
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| ORD ID | ord-22db604854c9438db3a67b3415eae414 |
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| 出典メモ | uspto-grants-2008_01 |
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