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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19949생성일: 2026년 10월 23일

Toluene → 4-{[Bis-(4-sulphamoyloxy-phenyl)-methyl]-[1,2,4]triazol-4-yl-amino}-benzonitrile

https://huagongshe.com/ko/reaction/19949

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Chlorosulfamic acidHCID 24499—
반응물4-([Bis-(4-hydroxy-phenyl)-methyl]-[1,2,4]triazol-4-yl-amino}-benzonitrileHCID 21976858—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매DimethylacetamideHCID 31374—
생성물4-{[Bis-(4-sulphamoyloxy-phenyl)-methyl]-[1,2,4]triazol-4-yl-amino}-benzonitrileHCID 21976886—

반응 단계

Sulphamoyl chloride solution in toluene (5 mL, 0.7 M, 3.5 mmol) was concentrated under reduced pressure (30° C. water bath temperature) to ca. 1 mL volume. The residue was cooled to 0° C. (ice bath) and N,N-dimethylacetamide (5 mL) was added. 4-{[Bis-(4-hydroxy-phenyl)-methyl]-[1,2,4]triazol-4-yl-amino}-benzonitrile (CAB2070, 250 mg, 0.65 mmol) was added to the colourless solution and the mixture was stirred for 18 h at, room temperature. Ethyl acetate (50 mL) and water (30 mL) were added to the solution, the organic layer was separated, washed with water (2×30 mL) and brine (20 mL), dried over sodium sulphate and concentrated under reduced pressure to give a white solid. The solid was dissolved in ethyl acetate and precipitated by addition of hexane. The white powder was filtered off and dried under high vacuum. Yield: 299 mg (85%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745472B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3a71e3aaa6c843ed9a29a7fb1e9c4aea
출처 메모uspto-grants-2010_06