関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzaldehyde | HCID 240 | — |
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | 3-(2-Aminoethyl)-5-(4-ethoxybenzyl)thiazolidine-2,4-dione | HCID 71697071 | — |
| 反応物 | 3-(2-(Tritylamino)ethyl)thiazolidine-2,4-dione | HCID 71697168 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 3-(2-Aminoethyl)-5-(phenylmethylidene)-1,3-thiazolidine-2,4-dione | HCID 1551244 | 48.1% |
反応手順
Benzaldehyde (63 μL, 0.62 mmol) and compound 29 (250 mg, 0.62 mmol) were dissolved in 10 mL of anhydrous ethanol at room temperature, and piperidine (7 μL, 0.062 mmol) was added to the reaction solution. The reaction mixture was stirred at 75° C. for 1 day and then allowed to cool down to room temperature until a yellow crystalline precipitate formed, and the solid was collected by filtration, washed with water and ethyl acetate, and dried to afford a white solid. Deprotection following the procedure of compound 6 gave the title compound 30a as a white solid (48.1%, 74 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09115122B2 |
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| 出典データセット | uspto-grants-2015_08 |
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| ORD ID | ord-1c0a01a673f2498fba074e97cbe46588 |
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| 出典メモ | uspto-grants-2015_08 |
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