戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 15028作成日:2026年10月24日

4-(Morpholin-4-yl)benzoic acid → 6-(4-Morpholinophenyl)-3-(3,4,5-trimethoxyphenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

https://huagongshe.com/ja/reaction/15028

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Morpholin-4-yl)benzoic acidHCID 345278—
反応物HCID 178488244HCID 178488244—
溶媒Phosphorus oxychlorideHCID 24813—
生成物6-(4-Morpholinophenyl)-3-(3,4,5-trimethoxyphenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazoleHCID 2495522824.4%

反応手順

A mixture of 4-morpholinobenzoic acid (86 mg, 0.42 mmol) and 4-amino-3-mercapto-5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazole (102 mg, 0.36 mmol) was refluxed in POCl3 (5 mL) for 2 h. The reaction mixture was cooled to room temperature and excess POCl3 was removed under vacuum. The residue was dissolved in ethyl acetate and washed with saturated NaHCO3. The organic layer was dried over anhydrous Na2SO4, filtered and concentrated. The crude product was purified by chromatography (80% ethyl acetate/hexane; 1 mL methanol/100 mL of solvent) to give the title compound as a yellow solid (40 mg, 0.088 mmol, 24%). 1H NMR (CDCl3): 7.78 (m, 2H), 7.73 (s, 2H), 6.98 (m, 2H), 4.00 (s, 6H), 3.94 (s, 3H), 3.89 (m, 4H), 3.41 (m, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732468B2
出典データセットuspto-grants-2010_06
ORD IDord-1a99ddf1b32949a193135c68e1c70694
出典メモuspto-grants-2010_06