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HRID 323030作成日:2026年10月25日

Triethylamine → n-(2-Hydroxy-4-nitrophenyl)-n'-(3-methoxy-2-thienyl)urea

https://huagongshe.com/reaction/323030

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Diphenylphosphoryl azideHCID 123414—
反応物3-Methoxythiophene-2-carboxylic acidHCID 1483475—
反応物2-Amino-5-NitrophenolHCID 4984721—
溶媒TolueneHCID 1140—
生成物n-(2-Hydroxy-4-nitrophenyl)-n'-(3-methoxy-2-thienyl)ureaHCID 2118472248%

反応条件

温度70 °C

反応手順

To a solution of 3-methoxy-2-thiophene carboxylic acid (example 11a, 200 mg, 1.27 mmol) in toluene, (PhO)2PON3 (0.33 mL) and triethylamine (1. 1 equiv., 0.25 mL) were added. The reaction mixture was stirred at 70° C. for 2 hours and cooled down to room temperature then 2-amino-5-nitrophenol was added. The reaction mixture was stirred at 70° C. overnight. The reaction mixture was partitioned between 5% citric acid and ethyl acetate. The organic layer was separated and the aqueous layer was extracted three times with ethyl acetate. The organic extracts were combined, dried over MgSO4, filtered and concentrated under reduced pressure. Chromatography of the resulting solid on silica gel (hexane:ethyl acetate; 1:1) gave the product (190 mg, 48%). 1H NMR (CD3OD/CDCl3): d 8.38 (d, 1H, J=5.0 Hz), 7.85 (dd, 1H, J=5.0 Hz and J=1.25 Hz), 7.76 (d, 1H, J=2.5 Hz), 6.9 (s, 2H), 3.95 (s, 3H); El-MS m/z 309 (M+H)+; Anal. (C12H11N3O5S) C, H, N.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211373B1
出典データセットuspto-grants-2001_04
ORD IDord-c406b686b9b4498daa885b644e06ad84
出典メモuspto-grants-2001_04