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HRID 1385343作成日:2026年10月27日

Triethylamine → n-(2-Hydroxy-5-nitrophenyl)-n'-(3-methoxy-2-thienyl)urea

https://huagongshe.com/reaction/1385343

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-4-NitrophenolHCID 3613389—
溶媒BenzeneHCID 241—
生成物n-(2-Hydroxy-5-nitrophenyl)-n'-(3-methoxy-2-thienyl)ureaHCID 1541148641%

反応手順

To a solution of 3-methoxy-2-thiophene carboxylic acid (200 mg, 1.27 mmol) in benzene, (PhO)2PON3 (0.33 mL), 2-amino-4-nitrophenol (195.7 mg, 1.27 mmol) and triethylamine (1.1 equiv., 0.25 mL) were added. The reaction mixture was stirred at reflux 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 a solid product (160 mg, 41%). mp: 172.6-173.0° C.; 1H NMR (CD3OD/CDCl3): d 8.96 (d, 1H, J=2.5 Hz), 7.74 (dd, 1H, J=5.0 Hz and J=1.25 Hz), 6.82 (d, 1H, J=7.5 Hz), 6.76 (s, 2H), 3.80 (s, 3H); EI-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US06262113B1
出典データセットuspto-grants-2001_07
ORD IDord-a5fbc6afe2554eec8c3b74d4d25ba84e
出典メモuspto-grants-2001_07