戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 627996作成日:2026年10月26日

Toluene → 3-(9-bromo-4,5-dihydrobenzo[b]thieno[2,3-d]oxepin-2-yl)-4-(2,4-difluorophenyl)-4H-1,2,4-triazole

https://huagongshe.com/reaction/627996

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Dimethylformamide dimethyl acetalHCID 78373—
反応物2,4-Difluorophenylhydrazine hydrochlorideHCID 2733301—
反応物9-Bromo-4,5-dihydro-6-oxa-1-thia-benzo[e]azulene-2-carboxylic acid amideHCID 66868537—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物3-(9-bromo-4,5-dihydrobenzo[b]thieno[2,3-d]oxepin-2-yl)-4-(2,4-difluorophenyl)-4H-1,2,4-triazoleHCID 57900350—

反応条件

温度100 °C

反応手順

A mixture of 9-bromo-4,5-dihydro-6-oxa-1-thia-benzo[e]azulene-2-carboxylic acid amide (340 mg), dimethylformamide dimethyl acetal (3 ml) and toluene (2.5 mL) was heated to 100° C. for 16 hours. The solvent was then reduced in vacuo and dissolved in acetic acid (3 ml) and water (0.3 mL) and to this was added 2,4-difluorophenylhydrazine hydrochloride (265 mg). The reaction mixture was heated to 100° C. for 3 hours. The reaction mixture was then cooled, and then diluted with dichloromethane, washed with sodium carbonate solution, dried (MgSO4) and the solvent removed in vacuo. Purification using flash chromatography yielded 293. NMR: (CDCl3): 3.15 (2H, t), 4.31 (2H, t), 6.82 (1H, d), 6.86 (1H, s), 7.08-7.13 (2H, m), one proton under chloroform peak, 7.72 (1H, s), 8.10 (1H, s)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09309265B2
出典データセットuspto-grants-2016_04
ORD IDord-b5f837d48fb44bcaa26e004513a3a65a
出典メモuspto-grants-2016_04