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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36203생성일: 2026년 10월 25일

Sodium hydride → 5-n-Butyl-2,4-dihydro-4-[[2'-[N-(4-morpholinecarbonyl)sulfamoyl]biphenyl-4-yl]methyl]-2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/36203

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4-Morpholinecarbonyl chlorideHCID 84810—
반응물5-n-Butyl-2,4-dihydro-4-[(2'-sulfamoylbiphenyl-4-yl)methyl]-2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-oneHCID 10346902—
용매TetrahydrofuranHCID 8028—
생성물5-n-Butyl-2,4-dihydro-4-[[2'-[N-(4-morpholinecarbonyl)sulfamoyl]biphenyl-4-yl]methyl]-2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-oneHCID 1993936825.9%

반응 단계

To a solution of 51.1 mg (0.0964 mmole) of 5-n-butyl-2,4-dihydro-4-[(2'-sulfamoylbiphenyl-4-yl)methyl]- 2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-one (from Example 16, Step C) in 0.2 ml of dry THF was added 4.6 mg (0.116 mmole) of sodium hydride (60% in oil), and the mixture was allowed to stir at room temperature under N2 for 4 hours. Next, 17 μl (21.6 mg, 0.145 mmole) of 4-morpholinecarbonyl chloride was added, and the solution was stirred under N2 at room temperature overnight. The reaction was quenched by addition of 2 ml of H2O followed by extraction with 3×5 ml of ethyl acetate. The combined organic extracts were washed with 2×5 ml of H2O and then with 5 ml of brine. After co-evaporation twice from toluene, the crude product was flash chromatographed on silica gel (gradient elution with 0.3-10% MeOH in CH2Cl2) to give 16.1 mg of the title compound as a whitish glass; satisfactory purity by TLC in 19:1 and 9:1 CH2Cl2 --MeOH; mass spectrum (FAB) m/e 682 (M+K)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05411980
출처 데이터셋uspto-grants-1995_05
ORD IDord-ba88eb7ccfd041bea5602986a6ac3ae8
출처 메모uspto-grants-1995_05