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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 520247생성일: 2026년 10월 24일

Triethylamine → 3-[(Z)-N-[(2-amino-1,3-thiazol-4-yl)methoxy]-C-phenylcarbonimidoyl]-2-methyl-1,2,4-oxadiazol-5-one

https://huagongshe.com/ko/reaction/520247

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Fluorophenyl chloroformateHCID 2733256—
반응물(2Z)-2-[(2-amino-1,3-thiazol-4-yl)methoxyimino]-N-hydroxy-N-methyl-2-phenylethanimidamideHCID 71626941—
용매DimethylformamideHCID 6228—
생성물3-[(Z)-N-[(2-amino-1,3-thiazol-4-yl)methoxy]-C-phenylcarbonimidoyl]-2-methyl-1,2,4-oxadiazol-5-oneHCID 71626945104.2%

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온도0 °C

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To a solution of (2Z)-2-{[(2-amino-1,3-thiazol-4-yl)methoxy]imino}-N-hydroxy-N-methyl-2-phenylethanimidamide (5.00 g, 16.37 mmol, 1 eq.) and triethylamine (2.28 ml, 16.37 mmol, 1 eq) in DMF (100 ml) at 0° C., was added dropwise 4-fluorophenyl chloroformate (28.58 g, 16.37 mmol, 1 eq.). After stirring at 0° C. for 1 hour, the reaction was quenched by addition of water (50 ml) and extracted with EtOAc (2×150 ml). The organics were combined, dried over MgSO4 and concentrated. The residue was purified by chromatography on silica gel to give 3-[(Z)-{[(2-amino-1,3-thiazol-4-yl)methoxy]imino}(phenyl)methyl]-2-methyl-1,2,4-oxadiazol-5(2H)-one (5.65 g, 96% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09326515B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-066e9ff338f24b359bec8ecd27eb832c
출처 메모uspto-grants-2016_05