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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 727010생성일: 2026년 10월 24일

1,2-Diamino-4,5-difluorobenzene → 5,6-difluoro-1H-1,3-benzodiazol-2-amine

https://huagongshe.com/ko/reaction/727010

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Diamino-4,5-difluorobenzeneHCID 2736755—
반응물BrCN MeCNHCID 131718759—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물5,6-difluoro-1H-1,3-benzodiazol-2-amineHCID 10678708—

반응 단계

To a stirred solution of 4.9 mL of 5M BrCN/MeCN in 50 mL of H2O, was added dropwise a solution of 3.515 g (24.389 mmole) of 10 in 50 mL of MeOH over 20 min. After the addition, stirring was continued at room temperature for 2 h. The reaction mixture was concentrated to ~50 mL arid was extracted with EtOAc (50 mL×3). The combined EtOAc solution was back washed with 100 mL of H2O and then discarded. The combined H2O phase was basified with sat. NaHCO3 solution (precipitation occurred) and was extracted again with EtOAc (70 mL×3). The EtOAc solution was dried (Na2SO4) and evaporated to dryness. The residue was suspended in 50 mL of CHCl3 and filtered. The yellowish solid was washed with portions of CHCl3 to give 3.40 g of 11. The filtrate and washings were evaporated to dryness and the procedure was repeated to give an additional 0.355 g of 11. The total yield of 11 was 3.755 g (91%). 1H NMR DMSO-d6) d 10.79 (br. s, 1, 1-NH). 7.06 (dd, 2, 4-H and 7-H, 3JF-H =11.0 Hz, 4JF-H =7.5 Hz), 6.30 (br. s, 2, 2-NH2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05712255
출처 데이터셋uspto-grants-1998_01
ORD IDord-e8560434d9754da1a13a3a0a9a8a0b79
출처 메모uspto-grants-1998_01