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HRID 1015620作成日:2026年10月27日

Nitrogen → 3-(2,4-Dichloro-benzylamino)-5-phenyl-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1015620

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物2,4-Dichlorobenzyl chlorideHCID 7212—
反応物Sodium hydrideHCID 24758—
反応物Methyl 3-amino-5-phenylthiophene-2-carboxylateHCID 700562—
溶媒DimethylformamideHCID 6228—
生成物3-(2,4-Dichloro-benzylamino)-5-phenyl-thiophene-2-carboxylic acid methyl esterHCID 20775754—

反応条件

温度0 °C

反応手順

Sodium hydride (60% dispersion in oil, 180 mg, 4,72 mmol) was added to an ice-cold solution of 3-Amino-5-phenyl-thiophene-2-carboxylic acid methyl ester (1000 mg, 4,29 mmol) in 25 ml of dimethylformamide in an atmosphere of N2. After 5 min, 2,4-dichloro-1-chloromethyl-benzene (755 mg, 3,86 mmol) was added to the solution and then the reaction mixture was stirred for 30 min at 0° C. and 30 min at room temperature. The mixture was partitioned between ether (20 mL) and water (20 mL) and the organic layer was separated. The aqueous phase was washed twice with ether (2×20 mL) and the combined ether layer was dried (MgSO4) and concentrated. The residue obtained was then purified by precipitation. The crude product was taken in 25 ml of ethyl acetate, a yellow precipitate came out which was filtered to obtain 3-(2,4-Dichloro-benzylamino)-5-phenyl-thiophene-2-carboxylic acid methyl ester, 835 mg (55%). 1H-NMR (DMSO, 400 MHz): 7.67 ppm (m, 2H, Haro); 7.44-7.35 ppm (m, 6H, Haro); 7.26 ppm (s, 1H, Haro); 4.63 ppm (d, 2H, N—CH2); 3.75 ppm (s, 3H, O—CH3)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07985769B2
出典データセットuspto-grants-2011_07
ORD IDord-65b53ab1a2b8493d92e4fc5a1c54452a
出典メモuspto-grants-2011_07