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HRID 390709作成日:2026年10月26日
Cesium carbonate → (NZ)-N-[5-methyl-3-(4-methylsulfanylphenyl)-1,3-thiazol-2-ylidene]pyrrolidine-1-carboxamide
https://huagongshe.com/reaction/390709
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 4-Bromothioanisole | HCID 66037 | — |
| 反応物 | 5-Chloro-1,10-phenanthroline | HCID 77865 | — |
| 反応物 | N-(5-methyl-1,3-thiazol-2-yl)pyrrolidine-1-carboxamide | HCID 47197229 | — |
| 反応物 | Water ammonium hydroxide | HCID 86589665 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | (NZ)-N-[5-methyl-3-(4-methylsulfanylphenyl)-1,3-thiazol-2-ylidene]pyrrolidine-1-carboxamide | HCID 42644648 | — |
反応手順
To a 4 mL vial equipped with a septum cap and stir bar was added N-(5-methyl-1,3-thiazol-2-yl)pyrrolidine-1-carboxamide (50 mg, 0.24 mmol), copper(I) trifluoromethanesulfonate benzene complex (23.8 mg, 0.05 mmol), 5-chloro-1,10-phenanthroline (20.3 mg, 0.09 mmol) and cesium carbonate (84.8 mg, 0.26 mmol). The mixture was placed under a nitrogen atmosphere. (4-Bromophenyl)(methyl)sulfane (0.28 mmol) in 1-methyl-2-pyrrolidinone (1.0 mL) was added to the mixture. The reaction mixture was heated at 120° C. for overnight. A solution of concentrated ammonium hydroxide/water (1:2, 1 mL) was added and the mixture was filtered and solvent removed under reduced pressure. The residue was purified by reverse phase HPLC (C8, gradient 10-100% acetonitrile/water/0.1% trifluoroacetic acid).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08383657B2 |
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| 出典データセット | uspto-grants-2013_02 |
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| ORD ID | ord-1cc60547cd994901bce749ede1d15e81 |
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| 出典メモ | uspto-grants-2013_02 |
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