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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12130생성일: 2026년 10월 25일

Hydrochloric Acid → 6-[N-(5-bromo(2-pyridyl))carbamoyl]-2,3,4-trimethoxyphenyl [4-(1-methyl(2-imidazolin-2-yl))phenyl]carboxamide

https://huagongshe.com/reaction/12130

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물N-MethylethylenediamineHCID 8014—
반응물N-{6-(N-(5-bromo(2-pyridyl))carbamoyl]-2,3,4-trimethoxyphenyl}(4-cyanophenyl)carboxamideHCID 22596311—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물6-[N-(5-bromo(2-pyridyl))carbamoyl]-2,3,4-trimethoxyphenyl [4-(1-methyl(2-imidazolin-2-yl))phenyl]carboxamideHCID 2259631832%

반응 단계

To a solution of the compound of N-{6-[N-(5-bromo(2-pyridyl))carbamoyl]-2,3,4-trimethoxyphenyl}(4-cyanophenyl)carboxamide (680 mg, 1.33 mmol) in anhydrous methanol (5 ml) and ethyl acetate (10 ml) was saturated with hydrogen chloride gas at 0° C. The mixture was stirred at r.t. overnight. After the evaporated the solvent, the residue was dissolved in anhydrous methanol (5 ml) and N-methylethylenediamine (0.586 ml, 6.65 mmol) was added. The mixture was stirred under reflux condition for 2 hrs. After the evaporation of solvent, the crude residue was purified by RP-HPLC to give N-{6-[N-(5-bromo(2-pyridyl))carbamoyl]-2,3,4-trimethoxyphenyl}[4-(1-methyl(2-imidazolin-2-yl))phenyl]carboxamide as a white powder (240 mg, 32%). MS found for C26H26BrN5O5 M+=568, (M+2)+=570.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727982B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-7769d72acc204e3c94f7a4faf46f2404
출처 메모uspto-grants-2010_06