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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 601624생성일: 2026년 10월 26일

Water → [2-(3-Propyl-[1,2,4]oxadiazol-5-yl)-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/601624

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물Ethyl 3-{[(tert-butoxy)carbonyl]amino}propanoateHCID 15933116—
반응물HCID 178449909HCID 178449909—
용매DimethylformamideHCID 6228—
생성물[2-(3-Propyl-[1,2,4]oxadiazol-5-yl)-ethyl]-carbamic acid tert-butyl esterHCID 57466817—

반응 조건

온도0 °C

반응 단계

N-Hydroxy-butyramidine (0.425 g, 4.16 mmol) in DMF (2 ml) is added to a stirred suspension of sodium hydride (0.183 g of a 60% dispersion in oil, 4.58 mmol) in the presence of molecular sieves (0.4 g). The reaction flask is then immersed in a pre-heated oil bath at 50° C. and stirring continued for 5 min. 3-tert-Butoxycarbonylamino-propionic acid ethyl ester (0.904 g, 4.16 mmol) in DMF (2 ml) is added over 5 min followed by more DMF (2 ml). After 3 h at 50° C. the mixture is cooled to 0° C. and water (3 ml) is added. The mixture is allowed to warm to room temperature then filtered through Celite™ filter material, washing with ethyl acetate, and the solvent is removed. Purification by chromatography, eluting with DCM:MeOH (95:5 increasing to 85:15) affords the titled compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902375B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-7c4b4ec3643944bea55102e646b2ee01
출처 메모uspto-grants-2011_03