Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221378생성일: 2026년 10월 26일
Triethylamine → 4-(5-Pyridin-4-yl-4H-[1,2,4]triazol-3-ylmethoxy)piperidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/221378
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Isobutyl chloroformate | HCID 62365 | — |
| 반응물 | 2-((1-((Tert-butoxy)carbonyl)piperidin-4-yl)oxy)acetic acid | HCID 1502082 | — |
| 반응물 | N'-aminopyridine-4-carboximidamide | HCID 5160013 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 4-(5-Pyridin-4-yl-4H-[1,2,4]triazol-3-ylmethoxy)piperidine-1-carboxylic acid tert-butyl ester | HCID 178452155 | — |
반응 단계
A solution of 4-carboxymethoxypiperidine-1-carboxylic acid tert-butyl ester (Preparation 1, 255 mg, 0.952 mmol) and triethylamine (138 μl, 0.982 mmol) in toluene was cooled to 0° C. and isobutylchloroformate (127 μl, 0.982 mmol) added. After stirring at rt for 45 min 4-pyridinecarboximidic acid hydrazide (100 mg, 0.82 mmol) and 3 Å powdered molecular sieves (0.82 g) were added and the reaction heated under reflux for 18 h. On cooling, the mixture was filtered through celite, the filtrate evaporated and the residue dissolved in EtOAc (50 ml). After washing with saturated aqueous Na2CO3 (10 ml) and brine (10 ml), the solvent was removed and the residue purified by flash chromatography (EtOAc then 5% MeOH in EtOAc) to afford the title compound: RT=2.81 min; m/z (ES+)=360.1 [M+H]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08207147B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-630970dab58b4c2883be41289c975ffb |
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| 출처 메모 | uspto-grants-2012_06 |
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