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HRID 871912作成日:2026年10月27日

Glycolic Acid → 4-(5-Hydroxymethyl-[1,2,4]oxadiazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/871912

反応式

関与物質

役割名称HCID仕込み量
反応物Glycolic AcidHCID 757—
反応物TriethylamineHCID 8471—
反応物Sodium HydroxideHCID 14798—
反応物Isobutyl chloroformateHCID 62365—
反応物HCID 178451986HCID 178451986—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物4-(5-Hydroxymethyl-[1,2,4]oxadiazol-3-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 57986906—

反応手順

To a solution of hydroxy-acetic acid (1.67 g, 22 mmol), NEt3 (4.4 g, 44 mmol) in toluene (150 mL) was added isobutylchloroformate (6 g, 44 mmol) at 0° C. The mixture was stirred at room temperature for 1.5 hours. 4-(N-Hydroxycarbamimidoyl)-piperidine-1-carboxylic acid tert-butyl ester (5.35 g, 22 mmol) was added to the mixture. The mixture was heated under reflux overnight, and then cooled to room temperature; the mixture was washed successively with H2O and brine. After drying (Na2SO4), the solvent was removed. The residue was dissolved in THF (20 mL), and aqueous NaOH (10 mL, 10 mmol) was added. The mixture was stirred at room temperature for 2 hours and diluted with EtOAc (50 mL). The organic layer was washed with brine, after drying (Na2SO4), the solvent was removed in vacuo, and the residue was purified by silica column chromatography with EtOAc/hexanes to afford the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08975258B2
出典データセットuspto-grants-2015_03
ORD IDord-cd4495150a7a4a778a2ad9c964b627f1
出典メモuspto-grants-2015_03