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HRID 392284作成日:2026年10月24日

4-(Methylsulfanyl)thiophenol → HCID 22663926、化合物

https://huagongshe.com/ja/reaction/392284

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Methylsulfanyl)thiophenolHCID 136896—
反応物4-Chloropyridine-3-carbaldehydeHCID 14046674—
溶媒DimethylformamideHCID 6228—
生成物HCID 22663926HCID 22663926114.8%

反応条件

温度50 °C

反応手順

4-Chloronicotinaldehyde [prepared according to D. Albanese, M. Penso, M. Zenoni, Synthesis 1999, 1294-1296] (500 mg, 3.5 mmol), 4-methylsulfanyl-benzenethiol (606 mg, 3.88 mmol) potassium carbonate (586 mg, 4.24 mmol) and DMF (7 mL) were combined, the mixture was heated together at 50° C. for 1.5 h and then stirred at room temperature overnight. The solvent was removed in vacuo and the residue was partitioned between EtOAc (100 mL) and 10% aqueous K2CO3 (100 mL). The organic layer was dried (MgSO4) and evaporated to give the title compound (1.05 g) as a yellow oil. The 1H NMR spectrum showed the material to be of sufficient purity (90-95%) to be used without further purification; δH (CDCl3, 400 MHz) 2.54 (3H, s), 6.69 (1H, d), 7.35 (2H, d), 7.4 (2H, d), 8.35 (1H, d), 8.87 (1H, s), 10.24 (1H, s); MS m/z (TS+) 262 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06800652B2
出典データセットuspto-grants-2004_10
ORD IDord-8ac8bc349ff6476ab5621429455c11f1
出典メモuspto-grants-2004_10