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3-Methyl-5-[(4-nitrophenyl)methylidene]-1,3-thiazolidine-2,4-dione → 5-(4-Aminobenzyl)-3-methyl-1,3-thiazolane-2,4-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Methyl-5-[(4-nitrophenyl)methylidene]-1,3-thiazolidine-2,4-dione | HCID 1482884 | — |
| 触媒 | HCID 178418390 | HCID 178418390 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-(4-Aminobenzyl)-3-methyl-1,3-thiazolane-2,4-dione | HCID 2768373 | 79.4% |
反応手順
A mixture of 3-methyl-5-(4-nitrobenzylidene)-1,3-thiazolidine-2,4-dione (1.0 g), 5% palladium carbon (1.0 g) and tetrahydrofuran (150 mL) was subjected to catalytic reduction under hydrogen pressure of 5.0 kgf·cm−2. The catalyst was removed by filtration, and the filtrate was concentrated to give 5-(4-aminobenzyl)-3-methyl-1,3-thiazolidine-2,4-dione as colorless crystals (0.71 g, yield 79%). Recrystallization thereof from ethyl acetate-hexane gave colorless prism crystals. melting point: 91-92° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07423159B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-45c08b9c0289483abe2788e113b3c415 |
| 出典メモ | uspto-grants-2008_09 |