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HRID 724850作成日:2026年10月26日

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

https://huagongshe.com/reaction/724850

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Diamino-4,5-difluorobenzeneHCID 2736755—
反応物BrCN MeCNHCID 131718759—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物5,6-difluoro-1H-1,3-benzodiazol-2-amineHCID 10678708—

反応手順

To a stirred solution of 4.9 mL of 5M BrCN/MeCN in 55 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 and 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05705490
出典データセットuspto-grants-1998_01
ORD IDord-b443ec8a8ae84d33a9edb9acbfcfa009
出典メモuspto-grants-1998_01