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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Benzo-1,3-dioxole-5-acetic acid | HCID 76115 | — |
| 반응물 | 2-Thiophenecarbonyl chloride | HCID 78928 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Thiocarbohydrazide | HCID 2724189 | — |
| 용매 | Chloride | HCID 312 | — |
| 용매 | Dichloromethane methanol | HCID 21226129 | — |
| 생성물 | 3-((Benzo[d][1,3]dioxol-5-yl)methyl)-6-(thiophen-2-yl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole | HCID 16736061 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07728017B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-ecce3c714f654f259f67249d6ff0a797 |
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| 출처 메모 | uspto-grants-2010_06 |
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