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HRID 221378作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Isobutyl chloroformateHCID 62365—
反応物2-((1-((Tert-butoxy)carbonyl)piperidin-4-yl)oxy)acetic acidHCID 1502082—
反応物N'-aminopyridine-4-carboximidamideHCID 5160013—
溶媒TolueneHCID 1140—
生成物4-(5-Pyridin-4-yl-4H-[1,2,4]triazol-3-ylmethoxy)piperidine-1-carboxylic acid tert-butyl esterHCID 178452155—

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207147B2
出典データセットuspto-grants-2012_06
ORD IDord-630970dab58b4c2883be41289c975ffb
出典メモuspto-grants-2012_06