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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12442생성일: 2026년 10월 25일

Benzo-1,3-dioxole-5-acetic acid → 3-((Benzo[d][1,3]dioxol-5-yl)methyl)-6-(thiophen-2-yl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

https://huagongshe.com/reaction/12442

반응식

참여 물질

역할이름HCID투입량
반응물Benzo-1,3-dioxole-5-acetic acidHCID 76115—
반응물2-Thiophenecarbonyl chlorideHCID 78928—
반응물Sodium BicarbonateHCID 516892—
반응물ThiocarbohydrazideHCID 2724189—
용매ChlorideHCID 312—
용매Dichloromethane methanolHCID 21226129—
생성물3-((Benzo[d][1,3]dioxol-5-yl)methyl)-6-(thiophen-2-yl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazoleHCID 16736061—

반응 조건

온도170 °C

반응 단계

As shown in FIG. 2, 2-(benzo[d][1,3]dioxol-5-yl)acetic acid (1 mmol) and thiocarbonohydrazide (1.5 mmol) were heated at 170° C. for 15 min. The mixture was cooled and taken up in 5% MeOH/CH2Cl2 and saturated NaHCO3. The organics were washed with water, saturated NaCl, dried over Na2SO4, and concentrated in vacuo. The resulting 5-((benzo[d][1,3]dioxol-5-yl)methyl)-4H-4-amino-3-mercapto-1,2,4-triazole (compound 1001) was used as is in the next reaction. Accordingly, a mixture of compound 1001 and thiopene-2-carbonyl chloride (0.176 g, 1.2 mmol) suspended in excess phoshoryl chloride (˜10 mL) was refluxed 5 hours. The excess phoshoryl chloride was removed under reduced pressure and the subsequent residue was mixed with crushed ice. The solids were filtered, washed with water, and dried in vaciio. Purification by reversed-phase HPLC produced pure 3-((benzo[d][1,3]dioxol-5-yl)methyl)-6-(thiophen-2-yl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole (compound 2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728017B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ecce3c714f654f259f67249d6ff0a797
출처 메모uspto-grants-2010_06