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HRID 2053559作成日:2026年10月26日

3,4-Difluorobenzyl Chloride → 2-[(3,4-Difluorobenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole Hydrochloride

https://huagongshe.com/reaction/2053559

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-Difluorobenzyl ChlorideHCID 2736954—
反応物cis-4,5-Diphenylimidazolidine-2-thioneHCID 45258634—
溶媒EthanolHCID 702—
生成物2-[(3,4-Difluorobenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole HydrochlorideHCID 6856964363.2%

反応手順

A mixture of intermediate 25 (200 mg, 0.786 mmol) and 3,4-difluorobenzyl chloride (0.255 mg, 1.57 mmol) in abs. EtOH (2 mL) is heated at 95° C. for 24 h. The reaction mixture is cooled to RT, evaporated to dryness, and the residue suspended in Et2O. The insoluble material is filtered to give 207 mg of the product 214. 1H NMR (DMSO-d6) δ 11.38 (s, 2H), 7.90-7.65 (m, 1H), 7.65-7.40 (m, 2H), 7.20-6.90 (m, 6H), 6.90-6.65 (m, 4H), 5.79 (s, 2H), 4.85 (s, 2H); MS: m/z 381 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07326792B2
出典データセットuspto-grants-2008_02
ORD IDord-f57ff2190632437ab7f03fccfce13154
出典メモuspto-grants-2008_02