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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1015620생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1015620

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물2,4-Dichlorobenzyl chlorideHCID 7212—
반응물Sodium hydrideHCID 24758—
반응물Methyl 3-amino-5-phenylthiophene-2-carboxylateHCID 700562—
용매DimethylformamideHCID 6228—
생성물3-(2,4-Dichloro-benzylamino)-5-phenyl-thiophene-2-carboxylic acid methyl esterHCID 20775754—

반응 조건

온도0 °C

반응 단계

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)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07985769B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-65b53ab1a2b8493d92e4fc5a1c54452a
출처 메모uspto-grants-2011_07