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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43043생성일: 2026년 10월 24일

Triethylamine → 8-(2,6-Dichloro-3,5-dimethoxy-phenyl)-quinoxaline-5-carboxylic acid [4-(4-ethyl-piperazin-1-yl)-phenyl]-amide

https://huagongshe.com/ko/reaction/43043

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-(4-Ethylpiperazin-1-yl)anilineHCID 936738—
반응물Propylphosphoric anhydrideHCID 16167369—
반응물8-(2,6-Dichloro-3,5-dimethoxy-phenyl)quinoxaline-5-carboxylic acidHCID 59292838—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물8-(2,6-Dichloro-3,5-dimethoxy-phenyl)-quinoxaline-5-carboxylic acid [4-(4-ethyl-piperazin-1-yl)-phenyl]-amideHCID 44513528—

반응 단계

A mixture of propylphosphonic anhydride (50% in DMF, 0.31 mL, 0.53 mmol, 2 equiv), 8-(2,6-dichloro-3,5-dimethoxy-phenyl)-quinoxaline-5-carboxylic acid (100 mg, 0.26 mmol) (Step 1.1), 4-(4-ethylpiperazin-1-yl)-aniline (Step 1.9) (65 mg, 0.32 mmol, 1.2 equiv), DMAP (2 mg), and Et3N (0.37 mL, 2.65 mmol, 10 equiv) in DMF (2.0 mL), was stirred for 18 h at rt, under an argon atmosphere. The reaction mixture was diluted with EtOAc and H2O. The aqueous layer was separated and extracted with EtOAc. The combined organic phase was washed with brine, dried (Na2SO4), filtered and concentrated. The residue was purified by trituration in Et2O to afford the title compound as a yellow solid: ES-MS: 565.9 [M+H]+; tR=4.26 min (System 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536175B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-28d5a761e9ea4cb595861a2c4423f7ec
출처 메모uspto-grants-2013_09