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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1364500생성일: 2026년 10월 25일

Succinic anhydride → 4-{4-[5-amino-1-(2,6-difluoro-benzoyl)-1H-[1,2,4]triazol-3-ylamino]-benzenesulfonylamino}-4-oxo-butyric acid

https://huagongshe.com/reaction/1364500

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참여 물질

역할이름HCID투입량
반응물Succinic anhydrideHCID 7922—
반응물Jnj-7706621HCID 5330790—
반응물Potassium tert-butoxideHCID 23665647—
촉매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
생성물4-{4-[5-amino-1-(2,6-difluoro-benzoyl)-1H-[1,2,4]triazol-3-ylamino]-benzenesulfonylamino}-4-oxo-butyric acidHCID 1159843231%

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온도0 °C

반응 단계

To a nitrogen purged flask was added 4-[5-amino-1-(2,6-difluorobenzoyl)-1H-[1,2,4]triazol-3-ylamino]-benzenesulfonamide Compound 1a (0.10 g, 0.25 mmol) and THF (10 mL). The mixture was cooled to 0° C. and potassium tert-butoxide (0.28 mL, 1.0 M solution in THF) was added dropwise. After addition the mixture was stirred at 0° C. for 1 hr, then succinic anhydride (28 mg in 5 mL THF, 0.28 mmol) was added dropwise. The stirring was continued for 30 min, then the mixture was warmed to rt and stirred overnight. A few drops of acetic acid was added, then the mixture was concentrated. The residue was purified by flash chromatography (silica gel, CH2Cl2:MeOH/8:2) to afford the desired product (39 mg, 31%) as a white solid. 1H NMR (300 MHz, CD3OD) δ 7.70 (d, 2H), 7.63 (m, 1H), 7.42 (d, 2H), 7.15 (t, 2H), 2.41 (br s, 4H); MS (ESI) m/z: 493 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07888380B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-970c51e705234409bcd2700beb27eb9c
출처 메모uspto-grants-2011_02