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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 517612생성일: 2026년 10월 26일

Benzaldehyde → 3-(2-Aminoethyl)-5-(phenylmethylidene)-1,3-thiazolidine-2,4-dione

https://huagongshe.com/reaction/517612

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물PiperidineHCID 8082—
반응물3-(2-Aminoethyl)-5-(4-ethoxybenzyl)thiazolidine-2,4-dioneHCID 71697071—
반응물3-(2-(Tritylamino)ethyl)thiazolidine-2,4-dioneHCID 71697168—
용매EthanolHCID 702—
생성물3-(2-Aminoethyl)-5-(phenylmethylidene)-1,3-thiazolidine-2,4-dioneHCID 155124448.1%

반응 조건

온도75 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115122B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-1c0a01a673f2498fba074e97cbe46588
출처 메모uspto-grants-2015_08