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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1807751생성일: 2026년 10월 24일

4-Nitrophenyl chloroformate → 1-(5-tert-Butylisoxazol-3-yl)-3-(2-fluoro-4-(4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperazine-1-carbonyl)phenyl)urea

https://huagongshe.com/ko/reaction/1807751

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참여 물질

역할이름HCID투입량
반응물4-Nitrophenyl chloroformateHCID 82129—
반응물3-Isoxazolamine, 5-(1,1-dimethylethyl)-HCID 171473—
반응물(4-Amino-3-fluorophenyl)(4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperazin-1-yl)methanoneHCID 86638550—
용매TetrahydrofuranHCID 8028—
생성물1-(5-tert-Butylisoxazol-3-yl)-3-(2-fluoro-4-(4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperazine-1-carbonyl)phenyl)ureaHCID 445121545.2%

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온도120 °C

반응 단계

(4-Amino-3-fluorophenyl)(4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperazin-1-yl)methanone (0.417 mmol, 0.2 g) and 4-nitrophenyl carbono-chloridate (0.417 mmol, 0.084 g) were combined and stirred in tetrahydrofuran (2 mL) at room temperature for 1 hour. 5-tert-Butylisoxazol-3-amine (1.252 mmol, 0.175 g) was added and the reaction heated in the microwave to 120° C. for 10 minutes. The solvent was removed at reduced pressure and the resulting residue purified by silica column chromatography (eluant dichloromethane/methanol 0% to 5%) to afford the title compound (14 mg). MS (ESI) m/z 646.5 [M+H]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08357679B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-da286ada38ad4812941d8e9424fecd87
출처 메모uspto-grants-2013_01