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Diisopropylethylamine → (3Z)-3-[3-(4-chlorophenyl)-1,3-thiazolidin-2-ylidene]-1-[(3-fluorophenyl)methyl]-1-methylurea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisopropylethylamine | HCID 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 iodide | HCID 87447829 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (3Z)-3-[3-(4-chlorophenyl)-1,3-thiazolidin-2-ylidene]-1-[(3-fluorophenyl)methyl]-1-methylurea | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08383657B2 |
| 出典データセット | uspto-grants-2013_02 |
| ORD ID | ord-8fa8ec507c26409c82d23e9ea08d68e4 |
| 出典メモ | uspto-grants-2013_02 |