참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzaldehyde | HCID 240 | — |
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | 3-(2-Aminoethyl)-5-(4-ethoxybenzyl)thiazolidine-2,4-dione | HCID 71697071 | — |
| 반응물 | 3-(2-(Tritylamino)ethyl)thiazolidine-2,4-dione | HCID 71697168 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 3-(2-Aminoethyl)-5-(phenylmethylidene)-1,3-thiazolidine-2,4-dione | HCID 1551244 | 48.1% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09115122B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-1c0a01a673f2498fba074e97cbe46588 |
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| 출처 메모 | uspto-grants-2015_08 |
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