돌아가기
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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Isobutyl chloroformateHCID 62365—
반응물2-((1-((Tert-butoxy)carbonyl)piperidin-4-yl)oxy)acetic acidHCID 1502082—
반응물N'-aminopyridine-4-carboximidamideHCID 5160013—
용매TolueneHCID 1140—
생성물4-(5-Pyridin-4-yl-4H-[1,2,4]triazol-3-ylmethoxy)piperidine-1-carboxylic acid tert-butyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207147B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-630970dab58b4c2883be41289c975ffb
출처 메모uspto-grants-2012_06