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HRID 38429作成日:2026年10月25日

Guanidine → 2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrile

https://huagongshe.com/reaction/38429

反応式

関与物質

役割名称HCID仕込み量
反応物GuanidineHCID 3520—
反応物Guanidine HydrochlorideHCID 5742—
反応物Benzenamine hydrochloride (1:1)HCID 8870—
反応物Sodium MethoxideHCID 10942334—
反応物3,3-Bis-dimethylamino-2-(4-ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-propionitrileHCID 59598706—
溶媒EthanolHCID 702—
生成物2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrileHCID 6705341355%

反応手順

3,3-Bis-dimethylamino-2-(4-ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-propionitrile (590 mg, 2 mmol) and aniline HCl (1.1 g, 9 mmol) in 5 mL absolute ethanol were heated at reflux for 2.0 hours. In a separate flask, guanidine HCl (0.850 mg., 9 mmol) and sodium methoxide solution (1.83 ml, 9 mmol, 4.9 molar solution in methanol) were mixed in 1 ml Ethanol. The guanidine solution was added to the reaction mixture via pipette, and the reaction mixture was heated to reflux for 5 hours, then cooled. Solvent was removed in vacuo, and the residue was, chromatographed (5% MeOH/methylene chloride/1% Na4OH) to give 368 mg 2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrile, 61%. Also present was 50 mg of 5-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-pyrimidine-2,4-diamine, 9%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524725B2
出典データセットuspto-grants-2013_09
ORD IDord-cc4c99025821491089fd53ccd157da18
出典メモuspto-grants-2013_09