Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81060생성일: 2026년 10월 25일
Ammonium Chloride → Methyl 4-(5-cyano-4-oxo-6-(4-phenoxyphenyl)-1,4-dihydropyridin-2-yl)benzoate
https://huagongshe.com/reaction/81060
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Methyl 4-(3-methoxy-3-oxopropanoyl)benzoate | HCID 3864207 | — |
| 반응물 | 3-Amino-3-(4-phenoxyphenyl)acrylonitrile | HCID 66927052 | — |
| 생성물 | Methyl 4-(5-cyano-4-oxo-6-(4-phenoxyphenyl)-1,4-dihydropyridin-2-yl)benzoate | HCID 66927073 | 65% |
반응 단계
A mixture of 3-amino-3-(4-phenoxyphenyl)acrylonitrile (0.517 g, 2.188 mmol) and methyl 4-(3-methoxy-3-oxopropanoyl)benzoate (2.068 g, 8.75 mmol) was microwaved at 230° C. for 20 min. After cooling to room temperature, the mixture was poured into saturated ammonium chloride (25 mL) and extracted with ethyl acetate (80 mL). The ethyl acetate phase was washed with saturated ammonium chloride (10 mL), water (10 mL), brine (5 mL), dried (MgSO4) and concentrated. Silica gel chromatography, eluting with 0-80% ethyl acetate in hexanes, gave impure products. The material was triturated with dichloromethane. The white solid was collected by filtration to give methyl 4-(5-cyano-4-oxo-6-(4-phenoxyphenyl)-1,4-dihydropyridin-2-yl)benzoate (0.598 g, 65% yield). 1H NMR (400 MHz, CDCl3) δ ppm 9.25 (1H, br. s), 8.17 (2H, br. s), 8.02 (1H, br. s), 7.71 (2H, br. s), 7.40 (2H, t, J=7.91 Hz), 7.24 (1H, br. s), 7.03-7.16 (4H, m), 6.62 (1H, br. s), 3.95 (3H, s); MS (ES+) m/z: 423 (M−H); LC retention time: 4.118 min (analytical HPLC Method A).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08846673B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-32dbd12d6901415b9c9597ee06267442 |
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| 출처 메모 | uspto-grants-2014_09 |
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