Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2043350생성일: 2026년 10월 26일
1H-Imidazole-4-carbaldehyde → (3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-(3H-imidazol-4-ylmethyl)-amine
https://huagongshe.com/reaction/2043350
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1H-Imidazole-4-carbaldehyde | HCID 76428 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 반응물 | (3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-amine | HCID 86620293 | — |
| 촉매 | Zincchloride | HCID 3007855 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | (3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-(3H-imidazol-4-ylmethyl)-amine | HCID 59728099 | 94% |
반응 단계
(3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-amine (0.10 g, 0.27 mmol) was dissolved in methanol (2 ml). Then 4-formylimidazole (0.13 g, 1.35 mmol), zinc chloride (0.15 g, 1.08 mmol) and sodium cyanoborohydride (0.05 g, 0.81 mmol) were added and the reaction mixture was allowed to stir at 40° C. overnight. After cooling, the reaction mixture was poured onto ammoniumchloride/ice and extracted with ethyl acetate (2 times 50 ml). The organic layer was dried over magnesium sulfate and evaporated. The residue was purified using flash chromatography (SiO2; eluent: methanol/dichloromethane=1:9) to yield an off-white gum (0.11 g, 94%); MS (ISP): 451.1 ([81Br M+H]+), 449.1 ([79Br M+H]+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08586617B2 |
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| 출처 데이터셋 | uspto-grants-2013_11 |
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| ORD ID | ord-8ed97e996e29403eb9a6aa0b5145949f |
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| 출처 메모 | uspto-grants-2013_11 |
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