反応式
[NH:1]1[CH:5]=[N:4][CH:3]=[N:2]1.[F:6][C:7]1[CH:14]=[CH:13][C:10]([CH2:11]Br)=[CH:9][CH:8]=1.N12CCCN=C1CCCCC2>C1COCC1>[F:6][C:7]1[CH:14]=[CH:13][C:10]([CH2:11][N:1]2[CH:5]=[N:4][CH:3]=[N:2]2)=[CH:9][CH:8]=1参加物
5
実験手順
To a stirred solution of 1,2,4-triazole (0.803 g, 11.6 mmol) in THF (100 mL) at 0° C. was added 4-fluorobenzyl bromide (2.0 g, 10.6 mmol), then 1,8-diazabicyclo[5.4.0]undec-7-ene (1.9 mL, 12.7 mmol) and the mixture was slowly warmed to room temperature. The solution was concentrated in vacuo, then purified by column chromatography (SiO2, MeOH/EtOAc, 5:95) to yield a white solid in 68% yield.
後処理
- concentrationThe solution was concentrated in vacuo
- custompurified by column chromatography (SiO2, MeOH/EtOAc, 5:95)
- customto yield a white solid in 68% yield
出典と根拠
- ORDレコード
- ord-61547b02120a4c1787c65a6c2cd437c3
- 出典データセット
- uspto-grants-2010_03
- 特許番号
- US07674813B2
関連ノート
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