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HRID 390701作成日:2026年10月23日

Diisopropylethylamine → (3Z)-3-[3-(4-chlorophenyl)-1,3-thiazolidin-2-ylidene]-1-[(3-fluorophenyl)methyl]-1-methylurea

https://huagongshe.com/ja/reaction/390701

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Benzenemethanamine, 3-fluoro-N-methyl-HCID 457577—
反応物(NZ)-N-[3-(4-chlorophenyl)-1,3-thiazolidin-2-ylidene]-3-methylimidazol-3-ium-1-carboxamide iodideHCID 87447829—
溶媒AcetonitrileHCID 6342—
生成物(3Z)-3-[3-(4-chlorophenyl)-1,3-thiazolidin-2-ylidene]-1-[(3-fluorophenyl)methyl]-1-methylureaHCID 44128476—

反応手順

To a solution of 1-({[(2Z)-3-(4-Chlorophenyl)-1,3-thiazolidin-2-ylidene]amino}carbonyl)-3-methyl-1H-imidazol-3-ium iodide (94 mg, 0.209 mmol, Example 25B) in dry acetonitrile (3 mL) were added diisopropylethylamine (0.040 mL, 0.230 mmol) and 1-(3-fluorophenyl)-N-methylmethanamine (0.032 mL, 0.230 mmol). The mixture was heated for 2 hours, and then cooled and concentrated under reduced pressure. The residue was purified by chromatography over silica using dichloromethane:methanol 95:5 as eluent to provide the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383657B2
出典データセットuspto-grants-2013_02
ORD IDord-8fa8ec507c26409c82d23e9ea08d68e4
出典メモuspto-grants-2013_02