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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 871912생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/871912

반응식

참여 물질

역할이름HCID투입량
반응물Glycolic AcidHCID 757—
반응물TriethylamineHCID 8471—
반응물Sodium HydroxideHCID 14798—
반응물Isobutyl chloroformateHCID 62365—
반응물HCID 178451986HCID 178451986—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물4-(5-Hydroxymethyl-[1,2,4]oxadiazol-3-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 57986906—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08975258B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-cd4495150a7a4a778a2ad9c964b627f1
출처 메모uspto-grants-2015_03