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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218323생성일: 2026년 10월 25일

N'-Hydroxybenzenecarboximidamide → 4-Benzyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)morpholine

https://huagongshe.com/reaction/218323

반응식

참여 물질

역할이름HCID투입량
반응물N'-HydroxybenzenecarboximidamideHCID 69186—
반응물DiisopropylethylamineHCID 81531—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물4-Benzylmorpholine-2-carboxylic acid hydrochlorideHCID 2776352—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-Benzyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)morpholineHCID 4695671177%

반응 단계

To a stirred solution of 4-benzyl-2-morpholinecarboxylic acid hydrochloride (intermediate 20, 1.5 g, 5.82 mmol) in N,N-dimethylformamide (10 ml) was added 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluroniumtetrafluoroborate (2.2 g, 6.98 mmol), 1-hydroxybenzotriazole hydrate (236 mg, 1.74 mmol) and N,N-diisopropylethylamine (5.1 ml, 29.1 mmol), and the reaction mixture was stirred at room temperature for 30 minutes. After the addition of N′-hydroxybenzamidine (792 mg, 5.82 mmol), the reaction mixture was stirred at room temperature for one hour, and then heated to 110° C. When the reaction was complete (checked by thin layer chromatography), excess reagent was decomposed by the addition of water and the aqueous layer was extracted with ethyl acetate. The extract was washed with water and brine, dried over magnesium sulfate, and concentrated in vacuo. The resulting residue was purified by column chromatography on silica gel, (eluent; 25% ethyl acetate in hexane) to afford 4-benzyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)morpholine (intermediate 21, 1.44 g, 77%) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198437B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-7841db3106c34e3c9282b61dd83d6901
출처 메모uspto-grants-2012_06