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HRID 18771作成日:2026年10月26日

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

https://huagongshe.com/reaction/18771

反応式

関与物質

役割名称HCID仕込み量
反応物3-Fluorobenzyl chlorideHCID 9974—
反応物cis-4,5-Diphenylimidazolidine-2-thioneHCID 45258634—
溶媒EthanolHCID 702—
生成物2-[(3-Fluorobenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole HydrochlorideHCID 6856887453.9%

反応手順

A mixture of intermediate 25 (200 mg, 0.786 mmol) and 3-fluorobenzyl chloride (0.190 mL, 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 169 mg of the product 219. 1H NMR (DMSO-d6) δ 11.39 (s, 2 H), 7.65-7.40 (m, 3 H), 7.35-7.20 (m, 1 H), 7.20-6.90 (m, 6 H), 6.90-6.65 (m, 4 H), 5.80 (s, 2 H), 4.85 (s, 2 H); MS: m/z 363 (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-ce4e4de4f0b84fa0911255f44f083ba1
出典メモuspto-grants-2010_06