Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12158생성일: 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/12158
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | N-Methylethylenediamine | HCID 8014 | — |
| 반응물 | N-{6-(N-(5-bromo(2-pyridyl))carbamoyl]-2,3,4-trimethoxyphenyl}(4-cyanophenyl)carboxamide | HCID 22596311 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 6-[N-(5-bromo(2-pyridyl))carbamoyl]-2,3,4-trimethoxyphenyl [4-(1-methyl(2-imidazolin-2-yl))phenyl]carboxamide | HCID 22596318 | 32% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07727981B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-958271ca3f154d7696885840af850fec |
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| 출처 메모 | uspto-grants-2010_06 |
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