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HRID 1951216作成日:2026年10月26日

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

https://huagongshe.com/reaction/1951216

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物Ethyl 3-{[(tert-butoxy)carbonyl]amino}propanoateHCID 15933116—
反応物HCID 178458070HCID 178458070—
溶媒DimethylformamideHCID 6228—
生成物[2-(3-Ethyl-[1,2,4]oxadiazol-5-yl)-ethyl]-carbamic acid tert-butyl esterHCID 57637085—

反応条件

温度0 °C

反応手順

N-Hydroxy-propionamidine (0.10 g, 1.15 mmol) in DMF (2 ml) is added to a stirred suspension of sodium hydride (0.05 g of a 60% dispersion in oil, 1.26 mmol) in DMF (20 ml) in the presence of molecular sieves (0.1 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 (0.25 g, 1.15 mmol) in DMF (2 ml) is added over 5 minutes. After 3 hours 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 hexane:ethyl acetate (3:1) affords the titled compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08404684B2
出典データセットuspto-grants-2013_03
ORD IDord-8b1e53775502443b96afc3ec26fb82f0
出典メモuspto-grants-2013_03