Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1386926생성일: 2026년 10월 27일
Sodium ethoxide → {3-[5-(4-methoxy-phenyl)-1H-[1,2,4]triazol-3-yl]-benzyl}-dimethylamine hydrochloride
https://huagongshe.com/reaction/1386926
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium ethoxide | HCID 2723922 | — |
| 반응물 | Ether hydrochloride | HCID 10953452 | — |
| 반응물 | 4-Methoxybenzamidine Hydrochloride | HCID 12326219 | — |
| 반응물 | 3-Dimethylaminomethyl-benzoic acid hydrazide | HCID 63571374 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | {3-[5-(4-methoxy-phenyl)-1H-[1,2,4]triazol-3-yl]-benzyl}-dimethylamine hydrochloride | HCID 21180376 | 25% |
반응 단계
To a stirred ethanolic suspension of 4-methoxybenzamidine hydrochloride salt (280 mg, 1.5 mmol, 1.5 eq.) was added over 3 minutes 1.2N NaOEt in ethanol (1.7 ml, 2 eq.) and stirring was continued for 30 min. at r.t. 3-Dimethylaminomethyl-benzoic acid hydrazide (193 mg, 1 mmol) in ethanol was then added at 20° C. and the mixture heated at reflux for 24 hrs. Upon cooling the product mixture was filtered, the solvent was evaporated and the residue subjected to preparative reversed phase-HPLC purification using a YMC ODS-AQ column (20×50 mm) and a (0.1% trifluoroacetic acid) water-acetonitrile gradient (25 ml/min.). The pure fractions were concentrated and the product obtained was converted to the hydrochloride salt by addition of excess 2N HCl/ether solution. Solvent evaporation and high vacuum drying afforded the title compound (86 mg, 0.25 mmol, 25% yield) as a white foam. MS: m/e=309.4 (M+H+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06265426B1 |
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| 출처 데이터셋 | uspto-grants-2001_07 |
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| ORD ID | ord-5141d93998634d50aca842132148e1d3 |
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| 출처 메모 | uspto-grants-2001_07 |
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