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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1879113생성일: 2026년 10월 24일

Triethylamine → Ethyl (3-chloro-4-{[(2-chloro-5-{[(3-chlorophenyl)methyl]oxy}phenyl)carbonyl]amino}-2-fluorophenyl)acetate

https://huagongshe.com/ko/reaction/1879113

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물Ethyl (4-amino-3-chloro-2-fluorophenyl)acetateHCID 59163335—
반응물2-Chloro-5-{[(3-chlorophenyl)methyl]oxy}benzoic acidHCID 59760049—
촉매DimethylformamideHCID 6228—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물Ethyl (3-chloro-4-{[(2-chloro-5-{[(3-chlorophenyl)methyl]oxy}phenyl)carbonyl]amino}-2-fluorophenyl)acetateHCID 5916336532.1%

반응 단계

A solution of 2-chloro-5-{[(3-chlorophenyl)methyl]oxy}benzoic acid (200 mg, 0.67 mmol) in dichloromethane (3 ml) was treated with oxalyl chloride (90 ul, 1.0 mmol) and DMF (1 drop). Effervescence was observed and the mixture was stirred at room temperature for 30 minutes. The solvent was then evaporated in vacuo and azeotroped with toluene. The resulting solid was dissolved in dichloromethane (3 ml) and treated with triethylamine (140 ul, 1.0 mmol) and a solution of ethyl (4-amino-3-chloro-2-fluorophenyl)acetate (230 mg, 1.0 mmol) in dichloromethane (2 ml). The mixture was stirred at room temperature for 2 hours. The mixture was then diluted with acetonitrile and purified by SCX cartridge eluting with acetonitrile. Fractions combined and evaporated, residue purified by MDAP to give the title compound as a white solid (110 mg). MS (ES+) m/z 510 [M+H]+ (C24H1935Cl3FNO4). 1H-NMR (400 MHz, d6-DMSO) δ 1.20 (3H, t, J 7.2), 3.81 (2H, s), 4.12 (2H, q, J 7.2), 5.20 (2H, s), 7.16-7.55 (9H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08314147B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-0e63bfbbd08547d4bf830891d0501af1
출처 메모uspto-grants-2012_11