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3-Pyridinecarboxaldehyde → (2R,4S)-2-(pyridin-3-yl)-1,3-thiazolidine-4-carboxylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| 反応物 | D-Cysteine | HCID 92851 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (2R,4S)-2-(pyridin-3-yl)-1,3-thiazolidine-4-carboxylic acid | HCID 22857565 | 54% |
反応手順
A solution of 1.07 g of pyridine-3-aldehyde and 1.21 g of D-cysteine in 60% v/v aqueous ethanol was heated under reflux for 4 hours. The mixture was cooled to room temperature and the resulting solid material was removed by filtration. The filtrate was concentrated by evaporation under reduced pressure, and 5 ml of ethanol were added to the resulting residue. Collecting the precipitated crystals by filtration gave 1.13 g (yield 54%) of the title compound, melting at 138°-139° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05470851 |
| 出典データセット | uspto-grants-1995_11 |
| ORD ID | ord-492bc5de6e494e6abeed9560618fc5f6 |
| 出典メモ | uspto-grants-1995_11 |