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HRID 18792作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/18792

反応式

関与物質

役割名称HCID仕込み量
反応物3-Phenoxybenzyl chlorideHCID 93291—
反応物cis-4,5-Diphenylimidazolidine-2-thioneHCID 45258634—
溶媒EthanolHCID 702—
生成物2-[(3-Phenoxybenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole HydrochlorideHCID 6856951994.1%

反応手順

A mixture of intermediate 25 (200 mg, 0.786 mmol) and 3-phenoxybenzyl chloride (343 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 350 mg of the product 241. 1H NMR (DMSO-d6) δ 11.25 (s, 2 H), 7.55-7.30 (m, 6 H), 7.30-7.25 (m, 1 H), 7.25-7.10 (m, 1 H), 7.15-6.90 (m, 6H), 6.90-6.70 (m, 4 H), 5.79 (s, 2 H), 4.81 (s, 2 H); MS: m/z 437 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741493B2
出典データセットuspto-grants-2010_06
ORD IDord-2a306ab3f06b42529fc294e67e46d6a9
出典メモuspto-grants-2010_06