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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Succinic anhydride | HCID 7922 | — |
| 반응물 | Jnj-7706621 | HCID 5330790 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 촉매 | Acetic Acid | HCID 176 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-{4-[5-amino-1-(2,6-difluoro-benzoyl)-1H-[1,2,4]triazol-3-ylamino]-benzenesulfonylamino}-4-oxo-butyric acid | HCID 11598432 | 31% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07888380B2 |
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| 출처 데이터셋 | uspto-grants-2011_02 |
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| ORD ID | ord-970c51e705234409bcd2700beb27eb9c |
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| 출처 메모 | uspto-grants-2011_02 |
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